Connexin 26 gene mutations in congenitally deaf children: Pitfalls for genetic counseling

Archives of Otolaryngology - Head and Neck Surgery

Volumn 127, Issue 8, 2001, Pages 927-933

  Marlin, Sandrine ^a   Garabédian, Éréa Noël ^a   Roger, Gilles ^a   Moatti, Lucien ^a   Matha, Nicole ^a   Lewin, Patricia ^b   Petit, Christine ^c   Denoyelle, Françoise ^a  

^a ARMAND TROUSSEAU HOSPITAL   (France)

^b LABORATOIRE CERBA   (France)

^c INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CONGENITAL DEAFNESS; FRAMESHIFT MUTATION; GENE MUTATION; GENETIC COUNSELING; GENOTYPE; HOMOZYGOSITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MISSENSE MUTATION; SEGREGATION ANALYSIS;

EID: 0034884213     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.127.8.927     Document Type: Article

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