Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13

American Journal of Medical Genetics

Volumn 76, Issue 5, 1998, Pages 395-401

  Kumar, Shrawan ^a   Marres, Henri A M ^b   Cremers, Cor W R J ^b   Kimberling, William J ^a  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Branchio otic type syndrome; Chromosome area 8q; Genetic linkage; Separate locus

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRANCHIAL DEFECT; BRANCHIOOTORENAL SYNDROME; CHONDRODYSPLASIA; CHROMOSOME 8Q; CLINICAL ARTICLE; FAMILY STUDY; GENETIC LINKAGE; HEARING LOSS; HUMAN; KIDNEY MALFORMATION; MANDIBULOFACIAL DYSOSTOSIS; NETHERLANDS; PEDIGREE; PRIORITY JOURNAL;

ALLELES; BRANCHIO-OTO-RENAL SYNDROME; CHROMOSOMES, HUMAN, PAIR 8; DEAFNESS; DNA; EAR; FEMALE; GENES; GENES, DOMINANT; GENETIC MARKERS; HUMANS; INFANT; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; SYNDROME;

EID: 0032513573     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980413)76:5<395::AID-AJMG6>3.0.CO;2-M     Document Type: Article

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