Keipert syndrome (nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28

American Journal of Medical Genetics, Part A

Volumn 143, Issue 19, 2007, Pages 2236-2241

  Amor, David J ^a,b,c   Dahl, Hans Henrik M ^a,c   Bahlo, Melanie ^d   Bankier, Agnes ^a,b,c  

^a MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

^c UNIVERSITY OF MELBOURNE   (Australia)

^d WALTER AND ELIZA HALL INSTITUTE OF MEDICAL RESEARCH   (Australia)

Author keywords

Deafness; Keipert syndrome; Linkage analysis; Nasodigitoacoustic syndrome; X chromosome

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME XQ; CLINICAL FEATURE; FACE MALFORMATION; FINGER MALFORMATION; HUMAN; KEIPERT SYNDROME; MALE; MICROSATELLITE MARKER; PEDIGREE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SYNDROME DELINEATION; X CHROMOSOME RECESSIVE INHERITANCE;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, X; DEAFNESS; FEMALE; FINGERS; GENETIC DISEASES, X-LINKED; HUMANS; INFANT; LINKAGE (GENETICS); MALE; NOSE; PEDIGREE; SYNDROME; TOES;

EID: 34848926088     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31917     Document Type: Article

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