Informacja

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

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""Vieira AR"" wg kryterium: Autor


Wyświetlanie 1-20 z 20
Tytuł :
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
Autorzy :
Shaffer JR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
LeClair J; Department of Computational and Systems Biology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, School of Public Health, Boston University, Boston, Massachusetts.
Carlson JC; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Feingold E; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Buxó CJ; Dental and Craniofacial Genomics Core, School of Dental Medicine, University of Puerto Rico, San Juan, Puerto Rico.
Christensen K; Department of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
Deleyiannis FWB; Department of Surgery, Plastic and Reconstructive Surgery, University of Colorado School of Medicine, Denver, Colorado.
Field LL; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Hecht JT; Department of Pediatrics, McGovern Medical School and School of Dentistry UT Health at Houston, Houston, Texas.
Moreno L; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa.
Orioli IM; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.
Padilla C; Department of Pediatrics, College of Medicine; and Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, The Philippines.; Philippine Genome Center, University of the Philippines System, Manila, The Philippines.
Vieira AR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Wehby GL; Department of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, Iowa.
Murray JC; Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa.
Weinberg SM; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Anthropology, Dietrich School of Arts and Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania.
Marazita ML; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Clinical and Translational Science, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Leslie EJ; Department of Human Genetics, Emory University School of Medicine, Emory University, Atlanta, Georgia.
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Mar; Vol. 179 (3), pp. 467-474. Date of Electronic Publication: 2018 Dec 24.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Genetic Association Studies*/methods
Genetic Predisposition to Disease*
Genetic Variation*
Regulatory Sequences, Nucleic Acid*
Brain/*abnormalities
Cleft Lip/*diagnosis
Cleft Lip/*genetics
Cleft Palate/*diagnosis
Cleft Palate/*genetics
Alleles ; Enhancer Elements, Genetic ; Genome-Wide Association Study ; Genotype ; Humans ; Phenotype ; Polymorphism, Single Nucleotide
SCR Disease Name :
Orofacial Cleft 1
Czasopismo naukowe
Tytuł :
Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.
Autorzy :
Leslie EJ; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Carlson JC; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Shaffer JR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Buxó CJ; School of Dental Medicine, University of Puerto Rico, San Juan, Puerto Rico.
Castilla EE; CEMIC: Center for Medical Education and Clinical Research, Buenos Aires, Argentina.; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.; Laboratory of Congenital Malformation Epidemiology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
Christensen K; Department of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
Deleyiannis FWB; Department of Surgery, Plastic and Reconstructive Surgery, University of Colorado School of Medicine, Denver, Colorado.
Field LL; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Hecht JT; Department of Pediatrics, McGovern Medical School and School of Dentistry UT Health at Houston, Houston, Texas.
Moreno L; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa.
Orioli IM; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Padilla C; Department of Pediatrics, College of Medicine; and Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, The Philippines.; Philippine Genome Center, University of the Philippines System, Manila, The Philippines.
Vieira AR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Wehby GL; Department of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, Iowa.
Feingold E; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Weinberg SM; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Murray JC; Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa.
Marazita ML; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Clinical and Translational Science, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2017 Jun; Vol. 173 (6), pp. 1531-1538. Date of Electronic Publication: 2017 Apr 19.
Typ publikacji :
Journal Article
MeSH Terms :
Basic Helix-Loop-Helix Transcription Factors/*genetics
Brain/*abnormalities
Cleft Lip/*genetics
Cleft Palate/*genetics
DNA Repair Enzymes/*genetics
Glycoproteins/*genetics
Membrane Proteins/*genetics
Repressor Proteins/*genetics
Alleles ; Brain/physiopathology ; Cleft Lip/physiopathology ; Cleft Palate/physiopathology ; European Continental Ancestry Group/genetics ; Exome/genetics ; Gene Frequency ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans ; Intercellular Signaling Peptides and Proteins ; Polymorphism, Single Nucleotide/genetics ; Risk Factors
SCR Disease Name :
Orofacial Cleft 1
Czasopismo naukowe
Tytuł :
The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.
Autorzy :
Mues G; Department of Biomedical Sciences, Texas A&M University-HSC Baylor College of Dentistry, Dallas, Texas.
Bonds J
Xiang L
Vieira AR
Seymen F
Klein O
D'Souza RN
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2014 Oct; Vol. 164A (10), pp. 2455-60. Date of Electronic Publication: 2014 Apr 03.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Ectodermal Dysplasia/*genetics
Tooth Abnormalities/*genetics
Wnt Proteins/*genetics
Alleles ; Anodontia ; Gene Frequency/genetics ; Heterozygote ; Humans ; Mutation/genetics ; Odontogenesis/genetics ; Phenotype ; Polymorphism, Single Nucleotide/genetics ; Tooth/pathology
SCR Disease Name :
Tooth Agenesis, Selective, 4
Czasopismo naukowe
Tytuł :
Risk of nonsyndromic cleft lip and palate in relatives of women with breast cancer.
Autorzy :
Martelli DR; Stomatology Clinic, Dental School, State University of Montes Claros, Montes Claros, Minas Gerais, Brazil.
Vieira AR
Fonseca AT
Coletta RD
Soares PB
Martelli-Júnior H
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2014 Jan; Vol. 164A (1), pp. 270-1. Date of Electronic Publication: 2013 Nov 20.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms/*complications
Cleft Lip/*complications
Cleft Palate/*complications
Breast Neoplasms/epidemiology ; Cleft Lip/epidemiology ; Cleft Palate/epidemiology ; Family ; Female ; Humans ; Risk
Czasopismo naukowe
Tytuł :
Risk of cancer in relatives of children born with isolated cleft lip and palate.
Autorzy :
Vieira AR; School of Dental Medicine, Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania 16261, USA. />Khaliq S
Lace B
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2012 Jun; Vol. 158A (6), pp. 1503-4. Date of Electronic Publication: 2012 May 14.
Typ publikacji :
Journal Article
MeSH Terms :
Cleft Lip*
Cleft Palate*
Neoplasms/*epidemiology
Adult ; Family ; Humans ; Prevalence ; Risk
Czasopismo naukowe
Tytuł :
Family history of cleft lip and palate in subjects diagnosed with leukemia.
Autorzy :
Jindal A; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Vieira AR
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2012 Mar; Vol. 158A (3), pp. 678-9. Date of Electronic Publication: 2012 Feb 02.
Typ publikacji :
Letter
MeSH Terms :
Cleft Lip/*genetics
Cleft Palate/*genetics
Leukemia/*diagnosis
Cleft Lip/complications ; Cleft Palate/complications ; Humans ; Leukemia/complications
Opinia redakcyjna
Tytuł :
Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate.
Autorzy :
Kantaputra PN; Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry, Chiang Mai University, Thailand. />Malaivijitnond S
Vieira AR
Heering J
Dötsch V
Khankasikum T
Sripathomsawat W
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2011 Jun; Vol. 155A (6), pp. 1432-6. Date of Electronic Publication: 2011 May 12.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cleft Lip/*genetics
Cleft Lip/*pathology
Cleft Palate/*genetics
Cleft Palate/*pathology
Genetic Predisposition to Disease/*genetics
Transcription Factors/*genetics
Tumor Suppressor Proteins/*genetics
Base Sequence ; Child, Preschool ; DNA Mutational Analysis ; Female ; Humans ; Infant ; Molecular Sequence Data ; Mutation, Missense/genetics ; Thailand
Czasopismo naukowe
Tytuł :
Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate.
Autorzy :
Letra A; Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, PA 15261, USA.
Menezes R
Govil M
Fonseca RF
McHenry T
Granjeiro JM
Castilla EE
Orioli IM
Marazita ML
Vieira AR
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2010 Jul; Vol. 152A (7), pp. 1701-10.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Genetic Association Studies*
Chromosomes, Human, Pair 9/*genetics
Cleft Lip/*genetics
Cleft Palate/*genetics
China ; Family ; Follow-Up Studies ; Genetic Markers ; Guatemala ; Haplotypes/genetics ; Humans ; Physical Chromosome Mapping ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Tytuł :
Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate.
Autorzy :
Neiswanger K; Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA 14219, USA. />Walker K
Klotz CM
Cooper ME
Bardi KM
Brandon CA
Weinberg SM
Vieira AR
Martin RA
Czeizel AE
Castilla EE
Poletta FA
Marazita ML
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2009 Dec; Vol. 149A (12), pp. 2673-9.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Cleft Lip/*complications
Cleft Lip/*pathology
Cleft Palate/*complications
Cleft Palate/*pathology
Lip/*abnormalities
Case-Control Studies ; Female ; Humans ; Male ; Phenotype ; Sex Characteristics
Czasopismo naukowe
Tytuł :
Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts.
Autorzy :
Vieira AR; Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Howe A
Murray JC
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2008 Nov 01; Vol. 146A (21), pp. 2828-30.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Cleft Lip/*genetics
Cleft Palate/*genetics
Glutamate Decarboxylase/*genetics
Receptors, GABA-A/*genetics
Adult ; Cleft Lip/metabolism ; Cleft Palate/metabolism ; Female ; Humans ; Iowa ; Male ; Philippines ; Polymorphism, Single Nucleotide ; Registries
Czasopismo naukowe
Tytuł :
Rethinking isolated cleft palate: evidence of occult lip defects in a subset of cases.
Autorzy :
Weinberg SM; Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15090, USA.
Brandon CA
McHenry TH
Neiswanger K
Deleyiannis FW
de Salamanca JE
Castilla EE
Czeizel AE
Vieira AR
Marazita ML
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2008 Jul 01; Vol. 146A (13), pp. 1670-5.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Cleft Lip/*complications
Cleft Lip/*diagnostic imaging
Cleft Palate/*complications
Cleft Palate/*diagnostic imaging
Facial Muscles/*abnormalities
Abnormalities, Multiple/diagnostic imaging ; Abnormalities, Multiple/genetics ; Cleft Lip/genetics ; Cleft Palate/genetics ; Facial Muscles/diagnostic imaging ; Female ; Humans ; Male ; Pedigree ; Retrospective Studies ; Ultrasonography ; Video Recording
Czasopismo naukowe
Tytuł :
Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies.
Autorzy :
Menezes R; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh 15261, USA.
Letra A
Ruff J
Granjeiro JM
Vieira AR
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2008 Jun 15; Vol. 146A (12), pp. 1614-7.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Genetic Linkage*
Fibroblast Growth Factors/*genetics
Mouth Abnormalities/*genetics
Tooth Abnormalities/*genetics
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Case-Control Studies ; Child ; Child, Preschool ; Female ; Humans ; Male ; Middle Aged ; Mouth Abnormalities/complications ; Polymorphism, Single Nucleotide ; Signal Transduction ; Tooth Abnormalities/complications
Czasopismo naukowe
Tytuł :
A genome wide linkage scan for cleft lip and palate and dental anomalies.
Autorzy :
Vieira AR; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA. />McHenry TG
Daack-Hirsch S
Murray JC
Marazita ML
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2008 Jun 01; Vol. 146A (11), pp. 1406-13.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Genome, Human*
Cleft Lip/*genetics
Cleft Palate/*genetics
Tooth Abnormalities/*genetics
Cytogenetic Analysis ; Humans ; Lod Score ; Microsatellite Repeats
Czasopismo naukowe
Tytuł :
Interferon regulatory factor 6 (IRF6) is associated with oral-facial cleft in individuals that originate in South America.
Autorzy :
Vieira AR; Department of Oral Biology and Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA. />Cooper ME
Marazita ML
Orioli IM
Castilla EE
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2007 Sep 01; Vol. 143A (17), pp. 2075-8.
Typ publikacji :
Case Reports; Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Review
MeSH Terms :
Cleft Lip/*genetics
Cleft Palate/*genetics
Interferon Regulatory Factors/*genetics
Female ; Genetic Variation ; Humans ; Indians, South American/genetics ; Male ; South America
Czasopismo naukowe
Tytuł :
A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23.
Autorzy :
Riley BM; Department of Pediatrics, University of Iowa, Iowa City, Iowa 52242, USA.
Schultz RE
Cooper ME
Goldstein-McHenry T
Daack-Hirsch S
Lee KT
Dragan E
Vieira AR
Lidral AC
Marazita ML
Murray JC
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2007 Apr 15; Vol. 143A (8), pp. 846-52.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 8*
Genetic Linkage*
Cleft Lip/*genetics
Cleft Palate/*genetics
Receptor, Fibroblast Growth Factor, Type 1/*genetics
Adaptor Proteins, Signal Transducing ; Chromosome Mapping ; Family Health ; Genomics ; Genotype ; Humans ; Lod Score ; Microsatellite Repeats ; Philippines/epidemiology ; Prevalence
Czasopismo naukowe
Tytuł :
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.
Autorzy :
Vieira AR; Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. />Modesto A
Meira R
Barbosa AR
Lidral AC
Murray JC
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2007 Mar 15; Vol. 143A (6), pp. 538-45.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Anodontia/*genetics
Interferon Regulatory Factors/*genetics
Receptor, Fibroblast Growth Factor, Type 1/*genetics
Adolescent ; Adult ; Algorithms ; Alleles ; Child ; Family Health ; Female ; Gene Frequency ; Genetic Markers ; Genetic Predisposition to Disease ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium ; MSX1 Transcription Factor/genetics ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Transforming Growth Factor alpha/genetics
Czasopismo naukowe
Tytuł :
PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.
Autorzy :
Avila JR; Department of Cytokine Biology, The Forsyth Institute and Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Jezewski PA
Vieira AR
Orioli IM
Castilla EE
Christensen K
Daack-Hirsch S
Romitti PA
Murray JC
Pokaż więcej
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2006 Dec 01; Vol. 140 (23), pp. 2562-70.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Genetic Variation*
Cell Adhesion Molecules/*genetics
Cleft Lip/*genetics
Cleft Palate/*genetics
Population/*genetics
Alleles ; Amino Acid Sequence ; Cell Adhesion Molecules/metabolism ; Cleft Lip/ethnology ; Cleft Palate/ethnology ; DNA Mutational Analysis ; Humans ; Linkage Disequilibrium ; Molecular Sequence Data ; Mutation ; Nectins
Czasopismo naukowe
    Wyświetlanie 1-20 z 20

    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