Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""trisomy 21"" wg kryterium: Temat

  Lista filtrów
Wyrównaj
Wyświetlanie 1-20 z 200
Tytuł:
A new contingent screening strategy increased detection rate of trisomy 21 in the first trimester
Autorzy:
Luo, WeiAff1, Aff2, Aff3
He, BinAff1, Aff2, Aff3
Han, DaiwenAff1, Aff2, Aff3
Yuan, LixingAff1, Aff2, Aff3
Tang, JunAff1, Aff2, Aff3
Pang, LingAff1, Aff2, Aff3
Zou, FeneAff1, Aff2, Aff3
Zhao, KaiAff1, Aff2, Aff3
Liu, ShanlingAff1, Aff2, Aff3
Hu, TingAff1, Aff2, Aff3, IDs12884023061151_cor10
Pokaż więcej
Źródło:
BMC Pregnancy and Childbirth. 23(1)
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prenatal diagnosis of Down syndrome combined with transient abnormal myelopoiesis in foetuses with a GATA1 gene variant: two case reports
Autorzy:
Hui Tang
Jingjing Hu
Ling Liu
Lijuan Lv
Jian Lu
Jiexia Yang
Jiaqi Lu
Zhenhui Chen
Chaoxiang Yang
Dan Chen
Jintao Fu
Jing Wu
Pokaż więcej
Temat:
Transient abnormal myelopoiesis
Down syndrome
Trisomy 21
GATA1
Prenatal diagnosis
Genetics
QH426-470
Źródło:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-8 (2023)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/1755-8166
Dostęp URL:
https://doaj.org/article/6275bd30a41d48e39dd0a7309fb94b4e  Link otwiera się w nowym oknie
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Mosaic trisomy 21 at amniocentesis associated with a favorable fetal outcome and perinatal progressive decrease of the trisomy 21 cell line
Autorzy:
Chih-Ping Chen
Shin-Wen Chen
Liang-Kai Wang
Schu-Rern Chern
Peih-Shan Wu
Fang-Tzu Wu
Yen-Ting Pan
Chen-Chi Lee
Li-Feng Chen
Chen-Wen Pan
Yun-Yi Chen
Wayseen Wang
Pokaż więcej
Temat:
Amniocentesis
Fetal outcome
Mosaic trisomy 21
Prenatal diagnosis
Gynecology and obstetrics
RG1-991
Źródło:
Taiwanese Journal of Obstetrics & Gynecology, Vol 62, Iss 1, Pp 132-136 (2023)
Opis pliku:
electronic resource
Relacje:
http://www.sciencedirect.com/science/article/pii/S1028455922003540; https://doaj.org/toc/1028-4559
Dostęp URL:
https://doaj.org/article/3f79b2e6bbe5418689f2306689df0862  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Mosaic trisomy 21 at amniocentesis in a twin pregnancy associated with a favorable fetal outcome, maternal uniparental disomy 21 and postnatal decrease of the trisomy 21 cell line
Autorzy:
Chih-Ping Chen
Te-Yao Hsu
Schu-Rern Chern
Peih-Shan Wu
Shin-Wen Chen
Liang-Kai Wang
Fang-Tzu Wu
Yen-Ting Pan
Chen-Chi Lee
Yun-Yi Chen
Wayseen Wang
Pokaż więcej
Temat:
Amniocentesis
Fetal outcome
Mosaic trisomy 21
Prenatal diagnosis
Gynecology and obstetrics
RG1-991
Źródło:
Taiwanese Journal of Obstetrics & Gynecology, Vol 62, Iss 1, Pp 137-141 (2023)
Opis pliku:
electronic resource
Relacje:
http://www.sciencedirect.com/science/article/pii/S1028455922003552; https://doaj.org/toc/1028-4559
Dostęp URL:
https://doaj.org/article/7e929e4dfc304c5ba6cb4f68ba77b064  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Novel Approaches to an Integrated Route for Trisomy 21 Evaluation.
Autorzy:
Buczyńska A; Clinical Research Centre, Medical University of Bialystok, 15-276 Bialystok, Poland.
Sidorkiewicz I; Clinical Research Centre, Medical University of Bialystok, 15-276 Bialystok, Poland.
Trochimiuk A; Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, 15-276 Bialystok, Poland.
Ławicki S; Department of Population Medicine and Civilization Diseases Prevention, Medical University of Bialystok, 15-276 Bialystok, Poland.
Krętowski AJ; Clinical Research Centre, Medical University of Bialystok, 15-276 Bialystok, Poland.; Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, 15-276 Bialystok, Poland.
Zbucka-Krętowska M; Department of Gynecological Endocrinology and Adolescent Gynecology, Medical University of Bialystok, 15-276 Bialystok, Poland.
Pokaż więcej
Źródło:
Biomolecules [Biomolecules] 2021 Sep 08; Vol. 11 (9). Date of Electronic Publication: 2021 Sep 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Genetic Testing*
Prenatal Diagnosis*
Down Syndrome/*diagnosis
Down Syndrome/*genetics
Biomarkers/metabolism ; Down Syndrome/metabolism ; Humans ; Metabolomics ; Proteomics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prenatal screening for trisomy 21: a comparative performance and cost analysis of different screening strategies.
Autorzy:
Huang T; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada. .; Prenatal Screening Ontario, Better Outcomes Registry & Network (BORN) Ontario, Ottawa, Ontario, Canada. .; Department of Obstetrics and Gynecology, University of Toronto, Toronto, Ontario, Canada. .
Gibbons C; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Rashid S; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada.
Priston MK; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada.
Bedford HM; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Mak-Tam E; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada.
Meschino WS; Genetics Program, North York General Hospital, 4001 Leslie Street, Toronto, Ontario, M2K 1E1, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Pokaż więcej
Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2020 Nov 23; Vol. 20 (1), pp. 713. Date of Electronic Publication: 2020 Nov 23.
Typ publikacji:
Journal Article
MeSH Terms:
Down Syndrome/*diagnosis
Noninvasive Prenatal Testing/*methods
Prenatal Diagnosis/*methods
Adult ; Cell-Free Nucleic Acids ; Costs and Cost Analysis ; Female ; Humans ; Maternal Serum Screening Tests/methods ; Nuchal Translucency Measurement/methods ; Ontario ; Patient Acceptance of Health Care ; Pregnancy ; Pregnancy Trimester, First
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Quantitative proteomic analysis of down syndrome biomarkers in maternal serum using isobaric tags for relative and absolute quantification (iTRAQ).
Autorzy:
Zhao SL; Department of Obstertrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Liu XW; Department of Obstertrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Wu SW; Department of Obstertrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Zheng YY; Department of Obstertrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Zhang WY; Department of Obstertrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Pokaż więcej
Źródło:
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology [Gynecol Endocrinol] 2020 Jun; Vol. 36 (6), pp. 489-495. Date of Electronic Publication: 2019 Dec 03.
Typ publikacji:
Journal Article
MeSH Terms:
Biomarkers/*blood
Down Syndrome/*diagnosis
Maternal Serum Screening Tests/*methods
Prenatal Diagnosis/*methods
Proteomics/*methods
Adult ; Biomarkers/analysis ; Case-Control Studies ; Down Syndrome/blood ; Female ; Humans ; Maternal Age ; Predictive Value of Tests ; Pregnancy
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Usefulness and reliability of cell free fetal DNA screening for main trisomies in case of atypical profile on first trimester maternal serum screening.
Autorzy:
Carrara J; Service de Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HP, 157 Rue de la Porte de Trivaux, 92140, Clamart, France. .; Université Paris Saclay, 91190, Saint-Aubin, France. .
Vivanti A; Service de Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HP, 157 Rue de la Porte de Trivaux, 92140, Clamart, France.; Université Paris Saclay, 91190, Saint-Aubin, France.
Jani JC; Department of Obstetrics and Gynecology, University Hospital Brugmann, Université Libre de Bruxelles, Brussels, Belgium.
Demain A; Service de Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HP, 157 Rue de la Porte de Trivaux, 92140, Clamart, France.
Costa JM; Laboratoire CERBA, Saint-Ouen l'Aumône, France.
Benachi A; Service de Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HP, 157 Rue de la Porte de Trivaux, 92140, Clamart, France.; Université Paris Saclay, 91190, Saint-Aubin, France.
Pokaż więcej
Źródło:
Journal of translational medicine [J Transl Med] 2019 Nov 28; Vol. 17 (1), pp. 398. Date of Electronic Publication: 2019 Nov 28.
Typ publikacji:
Journal Article
MeSH Terms:
Mass Screening*
Prenatal Diagnosis*
Cell-Free Nucleic Acids/*blood
Cell-Free Nucleic Acids/*genetics
Pregnancy Trimester, First/*blood
Pregnancy Trimester, First/*genetics
Trisomy/*genetics
Adult ; Cell-Free System ; Female ; Humans ; Logistic Models ; Middle Aged ; Pre-Eclampsia/blood ; Pre-Eclampsia/genetics ; Pregnancy ; Pregnancy Complications/blood ; Pregnancy Complications/diagnosis ; Pregnancy Complications/genetics ; Reproducibility of Results ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations.
Autorzy:
Gatinois V; Laboratoire de Génétique Chromosomique, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Bigi N; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Mousty E; Département de Gynécologie-Obstétrique, Hôpital Carémeau, CHU de Nîmes, Nîmes, France.
Chiesa J; Laboratoire de Cytologie Clinique et Cytogénétique, Hôpital Carémeau, CHU de Nîmes, Nîmes, France.
Musizzano Y; Laboratoire d'Anatomie et Cytologie Pathologique, Hôpital Gui-de-Chauliac, CHU de Montpellier, Montpellier, France.
Schneider A; Laboratoire de Génétique Chromosomique, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Lefort G; Laboratoire de Génétique Chromosomique, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Pinson L; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Gaillard JB; Laboratoire de Génétique Chromosomique, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Laboratoire de Cytologie Clinique et Cytogénétique, Hôpital Carémeau, CHU de Nîmes, Nîmes, France.
Ragon C; Laboratoire de Génétique Moléculaire et Cytogénétique, Hôpital du Bocage, CHU de Dijon, Dijon, France.
Perez MJ; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Tournaire M; Laboratoire de Génétique Chromosomique, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Blanchet P; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Corsini C; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Haquet E; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Callier P; Laboratoire de Génétique Moléculaire et Cytogénétique, Hôpital du Bocage, CHU de Dijon, Dijon, France.
Geneviève D; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Pellestor F; Laboratoire de Génétique Chromosomique, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Puechberty J; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2019 Nov; Vol. 7 (11), pp. e00895. Date of Electronic Publication: 2019 Sep 07.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Aneuploidy*
Mosaicism*
Tetrasomy*
Chromosomes, Human, Pair 21/*genetics
Heart Septal Defects/*diagnosis
Prenatal Diagnosis/*methods
Adult ; Amniocentesis ; Female ; Heart Septal Defects/genetics ; Humans ; Pregnancy
SCR Disease Name:
Complete atrioventricular septal defect
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prenatal Identification of Aberrant Right Subclavian Artery in Isolation: the Need for Further Genetic Work-Up?
Autorzy:
Reyhan Ayaz
Emine Göktas
Gurcan Turkyilmaz
Mehmet Resit Asoglu
Pokaż więcej
Temat:
Aberrant right subclavian artery
22q11.2 microdeletion
Aneuploidy
Trisomy 21
Prenatal diagnosis
Medicine
Źródło:
Acta Clinica Croatica, Vol 59., Iss 4., Pp 582-588 (2020)
Opis pliku:
electronic resource
Relacje:
https://hrcak.srce.hr/file/368712; https://doaj.org/toc/0353-9466; https://doaj.org/toc/1333-9451
Dostęp URL:
https://doaj.org/article/993e65d36ce3485699a9372318b83dfe  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Prenatal cell-free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory.
Autorzy:
Guy C; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Haji-Sheikhi F; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Rowland CM; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Anderson B; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Owen R; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Lacbawan FL; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Alagia DP; Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2019 Mar; Vol. 7 (3), pp. e545. Date of Electronic Publication: 2019 Jan 31.
Typ publikacji:
Evaluation Study; Journal Article
MeSH Terms:
Aneuploidy*
Cell-Free Nucleic Acids/*genetics
Chromosome Disorders/*diagnosis
Genetic Testing/*methods
Prenatal Diagnosis/*methods
Adult ; Cell-Free Nucleic Acids/chemistry ; Chromosome Disorders/genetics ; Female ; Genetic Testing/standards ; Humans ; Pregnancy ; Prenatal Diagnosis/standards ; Reproducibility of Results ; Sequence Analysis, DNA/methods ; Sequence Analysis, DNA/standards
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Improving women's knowledge about prenatal screening in the era of non-invasive prenatal testing for Down syndrome - development and acceptability of a low literacy decision aid.
Autorzy:
Smith SK; Psychosocial Research Group, Lowy Research Centre, C25, Prince of Wales Clinical School, Faculty of Medicine, UNSW Sydney, Corner High and Botany St, Kensington, Sydney New South Wales, 2033, Australia. .
Cai A; Psychosocial Research Group, Lowy Research Centre, C25, Prince of Wales Clinical School, Faculty of Medicine, UNSW Sydney, Corner High and Botany St, Kensington, Sydney New South Wales, 2033, Australia.
Wong M; Psychosocial Research Group, Lowy Research Centre, C25, Prince of Wales Clinical School, Faculty of Medicine, UNSW Sydney, Corner High and Botany St, Kensington, Sydney New South Wales, 2033, Australia.
Sousa MS; Psychosocial Research Group, Lowy Research Centre, C25, Prince of Wales Clinical School, Faculty of Medicine, UNSW Sydney, Corner High and Botany St, Kensington, Sydney New South Wales, 2033, Australia.; Centre for Applied Nursing Research, School of Nursing and Midwifery, Western Sydney University, Ingham, Sydney, Australia.; South Western Sydney Local Health District, Institute for Applied Medical Research, Sydney, Australia.
Peate M; Department of Obstetrics and Gynaecology, Royal Women's Hospital, University of Melbourne, Parkville, Australia.
Welsh A; School of Women's and Children's Health, UNSW Sydney, Sydney, Australia.; Department of Maternal-Fetal Medicine, Royal Hospital for Women, Sydney, Australia.
Meiser B; Psychosocial Research Group, Lowy Research Centre, C25, Prince of Wales Clinical School, Faculty of Medicine, UNSW Sydney, Corner High and Botany St, Kensington, Sydney New South Wales, 2033, Australia.
Kaur R; Psychosocial Research Group, Lowy Research Centre, C25, Prince of Wales Clinical School, Faculty of Medicine, UNSW Sydney, Corner High and Botany St, Kensington, Sydney New South Wales, 2033, Australia.
Halliday J; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Australia.
Lewis S; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Trevena L; Sydney School of Public Health, The University of Sydney, Sydney, Australia.
Yanes T; School of Psychiatry, Faculty of Medicine, UNSW Sydney, Sydney, Australia.
Barlow-Stewart K; Sydney Medical School, The University of Sydney, Sydney, Australia.
Barclay M; Women's Services, Liverpool Hospital, Sydney, Australia.; Western Sydney University, Parramatta, Sydney, Australia.
Pokaż więcej
Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2018 Dec 17; Vol. 18 (1), pp. 499. Date of Electronic Publication: 2018 Dec 17.
Typ publikacji:
Journal Article
MeSH Terms:
Pamphlets*
Down Syndrome/*diagnosis
Health Literacy/*methods
Pregnant Women/*education
Prenatal Diagnosis/*methods
Access to Information ; Adult ; Australia ; Female ; Humans ; Pregnancy ; Qualitative Research ; Teaching Materials
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Characteristics of prenatally detected right aortic arch cases in a single institution
Autorzy:
Melih Velipasaoglu
Metin Sentürk
Reyhan Ayaz
Barbaros Atesli
H. Mete Tanir
Pokaż więcej
Temat:
cardiac anomaly
right aortic arch
prenatal diagnosis
22q11.2 microdeletion
digeorge syndrome
trisomy 21
Gynecology and obstetrics
RG1-991
Źródło:
Journal of Obstetrics and Gynaecology, Vol 38, Iss 7, Pp 895-898 (2018)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/0144-3615; https://doaj.org/toc/1364-6893
Dostęp URL:
https://doaj.org/article/211949b9faa44ed4b9667d6477374f75  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Use of a patient decision aid for prenatal screening for Down syndrome: what do pregnant women say?
Autorzy:
Portocarrero ME; Population Health and Practice-Changing Research Group, CHU de Québec Research Centre, Quebec, Canada.
Giguère AM; Centre d'Excellence sur le Vieillissement de Québec, CHU de Québec Research Centre, Quebec, Canada.; Department of Family Medicine and Emergency Medicine, Laval University, Quebec, Canada.
Lépine J; Population Health and Practice-Changing Research Group, CHU de Québec Research Centre, Quebec, Canada.
Garvelink MM; Population Health and Practice-Changing Research Group, CHU de Québec Research Centre, Quebec, Canada.
Robitaille H; Population Health and Practice-Changing Research Group, CHU de Québec Research Centre, Quebec, Canada.
Delanoë A; Population Health and Practice-Changing Research Group, CHU de Québec Research Centre, Quebec, Canada.
Lévesque I; CHU de Québec, Hôpital St-François d'Assise, and Obstetrics and Gynecology Department, Faculty of Medicine, Laval University, Quebec, Canada.
Wilson BJ; Department of Epidemiology and Community Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Canada.
Rousseau F; Department of Molecular Biology, Medical Biochemistry and Pathology, Faculty of Medicine, Laval University, Quebec, Canada.; Health Technology Assessment and Evidence-based Laboratory Medicine, Quebec, Canada.
Légaré F; Population Health and Practice-Changing Research Group, CHU de Québec Research Centre, Quebec, Canada. .; Department of Family Medicine and Emergency Medicine, Laval University, Quebec, Canada. .; Population Health and Optimal Health Practice Research Group, CHU de Québec Research Centre, Hôpital St-François d'Assise, 10, rue de l'Espinay/D6-730, Quebec, G1L 3L5, Canada. .
Pokaż więcej
Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2017 Mar 20; Vol. 17 (1), pp. 90. Date of Electronic Publication: 2017 Mar 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Decision Making*
Decision Support Techniques*
Down Syndrome/*psychology
Pregnant Women/*psychology
Prenatal Diagnosis/*psychology
Adult ; Down Syndrome/diagnosis ; Female ; Health Personnel/psychology ; Humans ; Pregnancy ; Qualitative Research ; Quebec
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
The impact of national prenatal screening on the time of diagnosis and outcome of pregnancies affected with common trisomies, a cohort study in the Northern Netherlands.
Autorzy:
Bouman K; University of Groningen, University Medical Center Groningen, Department of Genetics, PO Box 30001, 9700 RB, Groningen, The Netherlands.
Bakker MK; University of Groningen, University Medical Center Groningen, Department of Genetics, PO Box 30001, 9700 RB, Groningen, The Netherlands. .; University of Groningen, University Medical Center Groningen, Department of Obstetrics, PO Box 30001, 9700 RB, Groningen, The Netherlands. .
Birnie E; University of Groningen, University Medical Center Groningen, Department of Genetics, PO Box 30001, 9700 RB, Groningen, The Netherlands.
Ter Beek L; University of Groningen, University Medical Center Groningen, Department of Genetics, PO Box 30001, 9700 RB, Groningen, The Netherlands.
Bilardo CM; University of Groningen, University Medical Center Groningen, Department of Obstetrics, PO Box 30001, 9700 RB, Groningen, The Netherlands.
van Langen IM; University of Groningen, University Medical Center Groningen, Department of Genetics, PO Box 30001, 9700 RB, Groningen, The Netherlands.
de Walle HE; University of Groningen, University Medical Center Groningen, Department of Genetics, PO Box 30001, 9700 RB, Groningen, The Netherlands.
Pokaż więcej
Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2017 Jan 05; Vol. 17 (1), pp. 4. Date of Electronic Publication: 2017 Jan 05.
Typ publikacji:
Evaluation Study; Journal Article
MeSH Terms:
Health Policy*
Time Factors*
Chromosome Disorders/*diagnosis
Mass Screening/*legislation & jurisprudence
Prenatal Diagnosis/*statistics & numerical data
Adult ; Chi-Square Distribution ; Down Syndrome/diagnosis ; Female ; Humans ; Netherlands ; Pregnancy ; Pregnancy Outcome ; Prenatal Diagnosis/methods ; Retrospective Studies ; Trisomy 13 Syndrome/diagnosis ; Trisomy 18 Syndrome/diagnosis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 1-20 z 200

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies