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Wyszukujesz frazę ""Genetics, Medical"" wg kryterium: Temat


Tytuł :
DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG).
Autorzy :
Murray MF; Department of Genetics, Yale School of Medicine, New Haven, CT, USA.
Giovanni MA; Genomics Consultant, Brookline, MA, USA.
Doyle DL; Washington State Department of Health (Ret.), Kent, WA, USA.
Harrison SM; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Lyon E; HudsonAlpha, Huntsville, AL, USA.
Manickam K; Clinical Pediatric, Nationwide Children's Hospital, Columbus, OH, USA.
Monaghan KG; GeneDx, Gaithersburg, MD, USA.
Rasmussen SA; Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA.; Department of Epidemiology, University of Florida College of Public Health and Health Professions and College of Medicine, Gainesville, FL, USA.
Scheuner MT; Division of Medical Genetics, Department of Pediatrics and Division of Hematology-Oncology, Department of Medicine, University of California San Francisco School of Medicine, San Francisco, CA, USA.; Clinical Genetics Program, San Francisco VA Health Care System, San Francisco, CA, USA.
Palomaki GE; Department of Pathology and Laboratory Medicine, Alpert Medical School, Brown University, Providence, RI, USA.; Women and Infants Hospital, Providence, RI, USA.
Watson MS; Self-employed, Washington, DC, USA.
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Corporate Authors :
ACMG Board of Directors
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Jun; Vol. 23 (6), pp. 989-995. Date of Electronic Publication: 2021 Mar 16.
Typ publikacji :
Journal Article
MeSH Terms :
Genetics, Medical*
Population Health*
DNA ; Genetic Testing ; Genome, Human ; Genomics ; Humans ; United States
Czasopismo naukowe
Tytuł :
DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG).
Autorzy :
Bean LJH; Department of Human Genetics, Emory University, Atlanta, GA, USA.
Scheuner MT; Division of Medical Genetics, Department of Pediatrics, and Division of Hematology-Oncology, Department of Medicine, University of California San Francisco School of Medicine, San Francisco, CA, USA.; Clinical Genetics Program, San Francisco VA Health Care System, San Francisco, CA, USA.
Murray MF; Department of Genetics, Yale School of Medicine, New Haven, CT, USA.
Biesecker LG; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Green RC; Harvard Medical School, Boston, MA, USA.; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Monaghan KG; GeneDx, Gaithersburg, MD, USA.
Palomaki GE; Department of Pathology and Laboratory Medicine, Alpert Medical School, Brown University, Providence, RI, USA.; Women and Infants Hospital, Providence, RI, USA.
Sharp RR; Biomedical Ethics Program, Mayo Clinic, Rochester, MN, USA.
Trotter TL; San Ramon Valley Primary Care Medical Group, San Ramon, CA, USA.
Watson MS; Self-employed, Washington, DC, USA.
Powell CM; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.; Division of Genetics and Metabolism, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Pokaż więcej
Corporate Authors :
ACMG Board of Directors
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Jun; Vol. 23 (6), pp. 979-988. Date of Electronic Publication: 2021 Mar 31.
Typ publikacji :
Journal Article
MeSH Terms :
Genetics, Medical*
DNA ; Genetic Testing ; Genome, Human ; Genomics ; Humans ; Mass Screening ; United States
Czasopismo naukowe
Tytuł :
Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Autorzy :
Spector E; Clinical Genetics and Metabolism, University of Colorado, School of Medicine, Aurora, CO, USA.; Precision Diagnostics Laboratory, Children's Hospital Colorado, Aurora, CO, USA.
Behlmann A; PerkinElmer Genomics, Duluth, GA, USA.
Kronquist K; Precision Diagnostics Laboratory, Children's Hospital Colorado, Aurora, CO, USA.
Rose NC; Department of Obstetrics and Gynecology, Adjunct, University of Utah Health Sciences Center, Salt Lake City, UT, USA.
Lyon E; Clinical Services Lab, HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
Reddi HV; Department of Pathology and Laboratory Medicine and Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.; Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, WI, USA.
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Corporate Authors :
ACMG Laboratory Quality Assurance Committee
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 May; Vol. 23 (5), pp. 799-812. Date of Electronic Publication: 2021 Apr 01.
Typ publikacji :
Journal Article
MeSH Terms :
Fragile X Syndrome*/diagnosis
Fragile X Syndrome*/genetics
Genetics, Medical*
Female ; Fragile X Mental Retardation Protein/genetics ; Genomics ; Humans ; Laboratories ; Mutation ; United States
Czasopismo naukowe
Tytuł :
Trainee perspectives of COVID-19 impact on medical genetics education.
Autorzy :
Pritchard AB; Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics, Michigan Medicine, Ann Arbor, MI, USA.
Sloan-Heggen C; Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics, Michigan Medicine, Ann Arbor, MI, USA.
Keegan CE; Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics, Michigan Medicine, Ann Arbor, MI, USA.
Quinonez SC; Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics, Michigan Medicine, Ann Arbor, MI, USA. .
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Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 May; Vol. 23 (5), pp. 956-962. Date of Electronic Publication: 2021 Feb 12.
Typ publikacji :
Journal Article
MeSH Terms :
COVID-19*
Education, Medical*
Genetics, Medical*
Internship and Residency*
Child ; Humans ; Pandemics ; SARS-CoV-2 ; Surveys and Questionnaires
Czasopismo naukowe
Tytuł :
A Case-Based Active Learning Session for Medical Genetics Resources.
Autorzy :
Anderson H; Associate Professor, Department of Internal Medicine and Department of Cell Biology and Human Anatomy, University of California Davis School of Medicine.
Studer AC; Health Science Librarian, Blaisdell Medical Library, University of California Davis School of Medicine.
Holm KN; Research Associate, Department of Biochemistry and Molecular Medicine, University of California Davis.
Suzuki A; Licensed and Certified Genetics Counselor, Division of Genomic Medicine, Department of Pediatrics, University of California Davis.
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Źródło :
MedEdPORTAL : the journal of teaching and learning resources [MedEdPORTAL] 2021 Apr 01; Vol. 17, pp. 11135. Date of Electronic Publication: 2021 Apr 01.
Typ publikacji :
Journal Article
MeSH Terms :
Genetics, Medical*/education
Problem-Based Learning*
Students, Medical*
Humans ; Surveys and Questionnaires
Czasopismo naukowe
Tytuł :
Opportunities and challenges for the computational interpretation of rare variation in clinically important genes.
Autorzy :
McInnes G; Biomedical Informatics Training Program, Stanford University, Stanford, CA 94305, USA.
Sharo AG; Biophysics Graduate Group, University of California, Berkeley, Berkeley, CA 94720, USA; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Koleske ML; Department of Bioengineering and Therapeutics, University of California, San Francisco, San Francisco, CA 94143, USA.
Brown JEH; Program in Bioethics, University of California, San Francisco, San Francisco, CA 94143, USA; Institute for Health & Aging, University of California, San Francisco, San Francisco, CA 94143, USA.
Norstad M; Program in Bioethics, University of California, San Francisco, San Francisco, CA 94143, USA; Institute for Health & Aging, University of California, San Francisco, San Francisco, CA 94143, USA.
Adhikari AN; Institute for Human Genetics, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA 94720, USA; Illumina, Inc., Foster City, CA 94404, USA.
Wang S; Paul G. Allen School of Computer Science & Engineering, University of Washington, Seattle, WA 98195, USA.
Brenner SE; Biophysics Graduate Group, University of California, Berkeley, Berkeley, CA 94720, USA; Institute for Human Genetics, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Halpern J; UCSF-UCB Joint Medical Program, School of Public Health, University of California, Berkeley, Berkeley, CA 94720, USA.
Koenig BA; Program in Bioethics, University of California, San Francisco, San Francisco, CA 94143, USA; Institute for Health & Aging, University of California, San Francisco, San Francisco, CA 94143, USA; Institute for Human Genetics, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Social & Behavioral Sciences, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Humanities & Social Sciences, University of California, San Francisco, San Francisco, CA 94143, USA.
Magnus DC; Stanford Center for Biomedical Ethics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Gallagher RC; Institute for Human Genetics, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94143, USA.
Giacomini KM; Department of Bioengineering and Therapeutics, University of California, San Francisco, San Francisco, CA 94143, USA.
Altman RB; Departments of Bioengineering & Genetics, Stanford University, Stanford, CA 94305, USA. Electronic address: .
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Źródło :
American journal of human genetics [Am J Hum Genet] 2021 Apr 01; Vol. 108 (4), pp. 535-548.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review
MeSH Terms :
Genetics, Medical*
Genomics*
Machine Learning*
Pharmacogenetics*
Precision Medicine*
Genetic Variation/*genetics
Metabolism, Inborn Errors/*genetics
Genome, Human/genetics ; Humans ; Infant, Newborn
Czasopismo naukowe
Tytuł :
Prenatal evaluation of fetuses with structural anomalies- is it time to shift from microarray to genome sequencing?
Autorzy :
Pan M; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Li DZ; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China. Electronic address: .
Pokaż więcej
Źródło :
Taiwanese journal of obstetrics & gynecology [Taiwan J Obstet Gynecol] 2021 Mar; Vol. 60 (2), pp. 389.
Typ publikacji :
Letter; Comment
MeSH Terms :
Exome*
Genetics, Medical*
Female ; Fetus ; Genomics ; Humans ; Microarray Analysis ; Pregnancy ; United States
Opinia redakcyjna
Tytuł :
Pediatric medical genetics house call: Telemedicine for the next generation of patients and providers.
Autorzy :
Cohen AJ; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
Shur N; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
Starin D; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
MacLeod E; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
Roshan Lal T; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
Leon E; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
Regier DS; Genetics and Metabolism, Children's National Hospital, Washington, District of Columbia, USA.
Pokaż więcej
Źródło :
American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2021 Mar; Vol. 187 (1), pp. 55-63. Date of Electronic Publication: 2021 Jan 11.
Typ publikacji :
Journal Article
MeSH Terms :
Genetics, Medical*/methods
House Calls/*statistics & numerical data
Pandemics/*statistics & numerical data
COVID-19/epidemiology ; COVID-19/virology ; Child ; Education, Medical ; Health Personnel ; Hospitals, Pediatric ; Humans ; Patient Care ; Quality Improvement ; Quality of Health Care ; SARS-CoV-2 ; Telemedicine/methods ; Telemedicine/statistics & numerical data
Czasopismo naukowe
Tytuł :
Correspondence on "The role of clinical response to treatment in determining pathogenicity of genomic variants" by Shen et al.
Autorzy :
Biesecker LG; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. .
Harrison SM; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Rehm HL; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
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Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Mar; Vol. 23 (3), pp. 586. Date of Electronic Publication: 2020 Nov 06.
Typ publikacji :
Letter; Comment
MeSH Terms :
Genetics, Medical*
Pathology, Molecular*
Consensus ; Genomics ; Humans ; United States ; Virulence
Opinia redakcyjna
Tytuł :
A wealth of discovery built on the Human Genome Project - by the numbers.
Autorzy :
Gates AJ
Gysi DM
Kellis M
Barabási AL
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Źródło :
Nature [Nature] 2021 Feb; Vol. 590 (7845), pp. 212-215.
Typ publikacji :
Historical Article; Journal Article
MeSH Terms :
Human Genome Project*/history
Genetics, Medical/*statistics & numerical data
Genome, Human/*genetics
DNA, Intergenic/genetics ; Drug Discovery ; Genes/genetics ; Genetic Diseases, Inborn/genetics ; Genetic Predisposition to Disease ; Genetics, Medical/trends ; History, 21st Century ; Humans ; Molecular Targeted Therapy ; Polymorphism, Single Nucleotide/genetics ; Proteins/genetics
Czasopismo naukowe
Tytuł :
Editorial: Medical genetics, expert medical testimony, and suspected child abuse cases: a call for evidence-based standards in clinic and the courtroom.
Autorzy :
Shur N; Division of Genetics and Metabolism, Rare Disease Institute, Children's National Hospital, Washington, District of Columbia.
Robin NH; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
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Źródło :
Current opinion in pediatrics [Curr Opin Pediatr] 2021 Feb 01; Vol. 33 (1), pp. 1-2.
Typ publikacji :
Editorial
MeSH Terms :
Child Abuse*/diagnosis
Genetics, Medical*
Child ; Expert Testimony ; Humans
Opinia redakcyjna
Tytuł :
Laboratory analysis of acylcarnitines, 2020 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Autorzy :
Miller MJ; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Cusmano-Ozog K; Department of Pathology, Stanford University Medical Center, Stanford, CA, USA.
Oglesbee D; Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Young S; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
Pokaż więcej
Corporate Authors :
ACMG Laboratory Quality Assurance Committee
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Feb; Vol. 23 (2), pp. 249-258. Date of Electronic Publication: 2020 Oct 19.
Typ publikacji :
Journal Article
MeSH Terms :
Genetics, Medical*
Laboratories*
Carnitine/analogs & derivatives ; Genomics ; Humans ; Infant, Newborn ; United States
Czasopismo naukowe
Tytuł :
Rapid deployment of a telemedicine care model for genetics and metabolism during COVID-19.
Autorzy :
Shur N; Children's National Hospital, Washington, District of Columbia, USA.
Atabaki SM; Children's National Hospital, Washington, District of Columbia, USA.
Kisling MS; Children's National Hospital, Washington, District of Columbia, USA.
Tabarani A; Children's National Hospital, Washington, District of Columbia, USA.
Williams C; Children's National Hospital, Washington, District of Columbia, USA.
Fraser JL; Children's National Hospital, Washington, District of Columbia, USA.
S Regier D; Children's National Hospital, Washington, District of Columbia, USA.
Summar M; Children's National Hospital, Washington, District of Columbia, USA.
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Corporate Authors :
Rare Disease Institute
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2021 Jan; Vol. 185 (1), pp. 68-72. Date of Electronic Publication: 2020 Oct 14.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Models, Organizational*
Pandemics*
COVID-19/*epidemiology
Delivery of Health Care/*organization & administration
Endocrinology/*organization & administration
Genetics, Medical/*organization & administration
Telemedicine/*organization & administration
Adolescent ; Adult ; Child ; Child, Preschool ; Delivery of Health Care/methods ; Delivery of Health Care/standards ; Endocrinology/education ; Female ; Genetic Counseling/methods ; Genetic Counseling/organization & administration ; Genetic Counseling/standards ; Genetic Diseases, Inborn/epidemiology ; Genetic Diseases, Inborn/therapy ; Genetic Testing/methods ; Genetic Testing/standards ; Genetics, Medical/education ; Humans ; Implementation Science ; Infant ; Infant, Newborn ; Internship and Residency/methods ; Internship and Residency/organization & administration ; Internship and Residency/standards ; Male ; Metabolic Diseases/epidemiology ; Metabolic Diseases/therapy ; Middle Aged ; Patient Safety ; Pilot Projects ; Program Evaluation ; Telemedicine/methods ; Young Adult
Czasopismo naukowe
Tytuł :
Lack of evidence to support recommendation for prenatal uniparental disomy (UPD) analysis following mosaic embryo transfer.
Autorzy :
Mounts EL; ORM Fertility, Portland, OR, USA.
Besser AG; NYU Langone Medical Center, NYU Fertility Center, New York, NY, USA. .
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Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Jan; Vol. 23 (1), pp. 230-231. Date of Electronic Publication: 2020 Aug 19.
Typ publikacji :
Letter; Comment
MeSH Terms :
Genetics, Medical*
Uniparental Disomy*/genetics
Diagnostic Techniques and Procedures ; Embryo Transfer ; Female ; Genomics ; Humans ; Pregnancy ; United States
Opinia redakcyjna
Tytuł :
Researchers at Cuba's National Medical Genetics Center: Pioneering Studies on COVID-19.
Autorzy :
Reed GA
Pokaż więcej
Źródło :
MEDICC review [MEDICC Rev] 2021 Jan; Vol. 23 (1), pp. 12-17. Date of Electronic Publication: 2021 Jan 30.
Typ publikacji :
Interview
MeSH Terms :
Genetics, Medical*
COVID-19/*genetics
National Health Programs/*organization & administration
SARS-CoV-2/*genetics
COVID-19/epidemiology ; Communicable Disease Control ; Cuba/epidemiology ; Female ; Humans ; Male ; Organizational Objectives ; Pandemics ; Population Surveillance
Tytuł :
Response to Mounts and Besser.
Autorzy :
Raca G; Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA, USA.; Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Shinawi M; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
Gaudio DD; Department of Human Genetics, The University of Chicago, Chicago, IL, USA.
Pokaż więcej
Corporate Authors :
American College of Medical Genetics and Genomics
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Jan; Vol. 23 (1), pp. 240-242. Date of Electronic Publication: 2020 Aug 20.
Typ publikacji :
Letter; Comment
MeSH Terms :
Genetics, Medical*
Uniparental Disomy*
Diagnostic Techniques and Procedures ; Diagnostic Tests, Routine ; Genomics ; Humans ; United States
Opinia redakcyjna
Tytuł :
Diversity, inclusion and equity in medical genetics: The time is now.
Autorzy :
Quintero-Rivera F; Department of Pathology and Laboratory Medicine, University of California Irvine School of Medicine, Irvine, California, USA.
Hisama FM; Department of Medicine (Medical Genetics), University of Washington School of Medicine, Seattle, Washington, USA.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Dec; Vol. 182 (12), pp. 2817-2819. Date of Electronic Publication: 2020 Oct 03.
Typ publikacji :
Editorial; Research Support, N.I.H., Extramural
MeSH Terms :
Cultural Diversity*
Delivery of Health Care*
Gender Equity*
Genetics, Medical*
Personnel Selection*
Ethnic Groups/*genetics
Humans
Raport
Tytuł :
[Cultivation of undergraduates' self-regulated learning ability in Medical Genetics based on PAD class].
Autorzy :
Yang YL; School of Basic Medicine, Kunming Medical University, Kunming 650500, China.
Luo L; School of Basic Medicine, Kunming Medical University, Kunming 650500, China.
Qian Y; The First Affiliated Hospital of Kunming Medical University, Kunming 650032, China.
Yang F; School of Basic Medicine, Kunming Medical University, Kunming 650500, China.
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Źródło :
Yi chuan = Hereditas [Yi Chuan] 2020 Nov 20; Vol. 42 (11), pp. 1133-1139.
Typ publikacji :
Journal Article
MeSH Terms :
Education, Medical*/standards
Genetics, Medical*/education
Learning*
Teaching*/standards
Humans ; Self-Control
Czasopismo naukowe
Tytuł :
Treatment of mucopolysaccharidosis type II (Hunter syndrome): a Delphi derived practice resource of the American College of Medical Genetics and Genomics (ACMG).
Autorzy :
McBride KL; Center for Cardiovascular Research and Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.; Department of Pediatrics, College of Medicine, Ohio State University, Columbus, OH, USA.
Berry SA; Division of Genetics and Metabolism, Departments of Pediatrics and Genetics, Cell Biology & Development, University of Minnesota, Minneapolis, MN, USA.
Braverman N; Department of Human Genetics and Pediatrics, McGill University, Montreal, QC, Canada.; Division of Medical Genetics, McGill University Health Center, Montreal, QC, Canada.
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Corporate Authors :
ACMG Therapeutics Committee
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2020 Nov; Vol. 22 (11), pp. 1735-1742. Date of Electronic Publication: 2020 Aug 03.
Typ publikacji :
Journal Article
MeSH Terms :
Genetics, Medical*
Mucopolysaccharidoses*
Mucopolysaccharidosis II*/diagnosis
Mucopolysaccharidosis II*/drug therapy
Mucopolysaccharidosis II*/genetics
Aged ; Enzyme Replacement Therapy ; Genomics ; Humans ; United States
Czasopismo naukowe
Tytuł :
How digital tools can advance quality and equity in genomic medicine.
Autorzy :
Bombard Y; Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health, Toronto, ON, Canada. .; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, ON, Canada. .
Hayeems RZ; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, ON, Canada.; Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Pokaż więcej
Źródło :
Nature reviews. Genetics [Nat Rev Genet] 2020 Sep; Vol. 21 (9), pp. 505-506.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Pandemics*
Software*
Coronavirus Infections/*epidemiology
Genetic Counseling/*organization & administration
Genetics, Medical/*organization & administration
Pneumonia, Viral/*epidemiology
Telemedicine/*organization & administration
Betacoronavirus/pathogenicity ; COVID-19/virology ; Coronavirus Infections/virology ; Genetics, Medical/instrumentation ; Genetics, Medical/methods ; Health Services Accessibility/ethics ; Health Services Accessibility/organization & administration ; Healthcare Disparities/ethics ; Humans ; Pneumonia, Viral/virology ; Quality Assurance, Health Care ; SARS-CoV-2 ; Telemedicine/instrumentation ; Telemedicine/methods
Czasopismo naukowe

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