Genetic heterogeneity associated with branchio-oto-renal syndrome [1]

American Journal of Medical Genetics

Volumn 83, Issue 3, 1999, Pages 207-208

  Kumar, S ^a   Kimberling, W J ^a   Marres, H A M ^a   Cremers, C W R J ^a  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRANCHIOOTORENAL SYNDROME; CLINICAL FEATURE; FAMILY STUDY; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; LETTER; MULTIPLE MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SYNDROME DELINEATION;

BRANCHIO-OTO-RENAL SYNDROME; GENETIC HETEROGENEITY; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MUTATION; NUCLEAR PROTEINS; PROTEIN-TYROSINE-PHOSPHATASE; TRANS-ACTIVATORS;

EID: 0033583212     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990319)83:3<207::AID-AJMG12>3.0.CO;2-A     Document Type: Letter

References (15)