Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome

American Journal of Human Genetics

Volumn 63, Issue 3, 1998, Pages 711-716

  Wilkin, Douglas J ^a   Szabo, Jinny K ^a   Cameron, Rhoda ^b   Henderson, Shirley ^c   Bellus, Gary A ^a,d,g   Mack, Michelle L ^a,e   Kaitila, Ilkka ^f   Loughlin, John ^c   Munnich, Arnold ^b   Sykes, Bryan ^c   Bonaventure, Jacky ^b   Francomano, Clair A ^a,d  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b INSERM   (France)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e GEORGE WASHINGTON UNIVERSITY   (United States)

^f HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^g UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FIBROBLAST GROWTH FACTOR RECEPTOR;

ACHONDROPLASIA; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA REPAIR; DNA REPLICATION; GENE MUTATION; HUMAN; NUCLEOTIDE SEQUENCE; OOCYTE DEVELOPMENT; PATERNAL AGE; PRIORITY JOURNAL; SPERMATOGENESIS;

EID: 0032231407     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302000     Document Type: Article

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