Genetical diagnosis in a family with X-linked hypohidrotic ectodermal dysplasia

Acta Academiae Medicinae Sinicae

Volumn 29, Issue 2, 2007, Pages 201-204

  Zhang, Hui ^a   Quan, Cheng ^a   Gao, Min ^a   Xiao, Feng Li ^a   Lu, Wen Sheng ^a   Shen, Yu Jun ^a   Zhou, Fu Sheng ^a   Yang, Sen ^a   Zhang, Xue Jun ^a  

^a ANHUI MEDICAL UNIVERSITY   (China)

Author keywords

Ectodermal dysplasia; ED1 gene; Mutation

Indexed keywords

ADENINE; ECTODYSPLASIN A; GUANINE;

AMINO ACID SEQUENCE; ARTICLE; CHINESE; CODING; CONTROLLED STUDY; EXON; FEMALE; GENE MUTATION; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; HYPOHIDROTIC ECTODERMAL DYSPLASIA; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; SEQUENCE ANALYSIS; X CHROMOSOME LINKED DISORDER;

ASIAN CONTINENTAL ANCESTRY GROUP; ECTODERMAL DYSPLASIA 1, ANHIDROTIC; ECTODYSPLASINS; GENETIC ASSOCIATION STUDIES; HUMANS; MUTATION; PEDIGREE;

EID: 34249667235     PISSN: 1000503X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

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