A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

Journal of Medical Genetics

Volumn 40, Issue 7, 2003, Pages 515-519

  Ruf, R G ^a   Berkman, J ^b   Wolf, M T F ^a   Nurnberg, P ^c,d   Gattas, M ^b   Ruf, E M ^e   Hyland, V ^f   Kromberg, J ^b   Glass, I ^g   Macmillan, J ^b   Otto, E ^a   Nurnberg, G ^c   Lucke, B ^h   Hennies, H C ^h   Hildebrandt, F ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

^c MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^d CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^e UNIVERSITY OF FREIBURG   (Germany)

^f QUEENSLAND HEALTH   (Australia)

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

^h NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRANCHIAL ARCH; BRONCHIO OTIC SYNDROME; CHROMOSOME 14Q; CHROMOSOME 8Q; CLINICAL ARTICLE; CONDUCTION DEAFNESS; EAR MALFORMATION; EYE ABSENT GENE; GENE; GENE LOCUS; GENE MAPPING; GENETIC DISORDER; GENETIC HETEROGENEITY; HEARING LOSS; HUMAN; KIDNEY MALFORMATION; LACRIMAL DUCT; ORGANOGENESIS; PERCEPTION DEAFNESS; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL;

EID: 0038163523     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.40.7.515     Document Type: Article

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