A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23

Human Molecular Genetics

Volumn 5, Issue 1, 1996, Pages 155-158

  Chaïb, Hassan ^a   Place, Christophe ^b   Salem, Nabiha ^b   Chardenoux, Sébastien ^a   Vincent, Christophe ^a   Weissenbach, Jean ^c   El Zir, Elie ^d   Loiselet, Jacques ^b   Petit, Christine ^a  

^a CNRS   (France)

^b SAINT JOSEPH UNIVERSITY   (Lebanon)

^c GÉNÉTHON   (France)

^d Sacre Coeur Hospital Baabda   (Lebanon)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 2P; CLINICAL ARTICLE; DNA POLYMORPHISM; FEMALE; GENE MAPPING; GENE SEGREGATION; GENETIC RECOMBINATION; HOMOZYGOSITY; HUMAN; HUMAN CELL; MALE; MARKER GENE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RECESSIVE INHERITANCE;

EID: 0030047197     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.1.155     Document Type: Article

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