Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4

Human Molecular Genetics

Volumn 5, Issue 9, 1996, Pages 1229-1235

  De Kok, Yvette J M ^a   Vossenaar, Erik R ^a   Cremers, Cor W R J ^a   Dahl, Niklas ^b   Laporte, Jocelyn ^c   Hu, Ling Jia ^c   Lacombe, Didier ^d   Fischel Ghodsian, Nathan ^e   Friedman, Rick A ^f   Parnes, Lorne S ^g   Thorpe, Peter ^h   Bitner Glindzicz, Maria ⁱ   Pander, Hans Jürgen ^j   Heilbronner, Helmut ^j   Graveline, Johanna ^k   Den Dunnen, Johan T ^l   Brunner, Han G ^a   Ropers, Hans Hilger ^a   Cremers, Frans P M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY CHILDREN S HOSPITAL   (Sweden)

^c INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^d HÔPITAL PELLEGRIN   (France)

^e CEDARS SINAI MEDICAL CENTER   (United States)

^f UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^g LONDON HEALTH SCIENCES CENTRE   (Canada)

^h James Paton Memorial Hospital   (Canada)

ⁱ UNIVERSITY COLLEGE LONDON   (United Kingdom)

^j Frauenklinik Berg   (Germany)

^k MOUNT SINAI MEDICAL CENTER   (United States)

^l LEIDEN UNIVERSITY   (Netherlands)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME XQ; CLINICAL ARTICLE; CONGENITAL DEAFNESS; COSMID; GENE; GENE DELETION; GENE MAPPING; HUMAN; MALE; MUTATION RATE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE TAGGED SITE; X CHROMOSOME LINKAGE;

BASE SEQUENCE; CHILD; CHROMOSOME MAPPING; GENE DELETION; HUMANS; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; X CHROMOSOME;

EID: 10144238527     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.9.1229     Document Type: Article

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