Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

The Gap Junction Communication Channel

1996 • 1,896 citations

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

1993 • 1,055 citations

Defective myosin VIIA gene responsible for Usher syndrome type IB

1995 • 1,051 citations

Genetic Epidemiology of Hearing Impairment

1991 • 941 citations

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

1992 • 692 citations

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1995 • 590 citations

Mutations of theConnexin43Gap-Junction Gene in Patients with Heart Malformations and Defects of Laterality

1995 • 376 citations

Genes responsible for human hereditary deafness: symphony of a thousand

1996 • 276 citations

Molecular biology and genetics of gap junction channels

1992 • 225 citations

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1993 • 223 citations

Structure of gap junction intercellular channels

1996 • 195 citations

Expression of gap junction proteins Cx26, Cx31.1, Cx37, and Cx43 in developing and mature rat epidermis

1994 • 147 citations

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

1994 • 133 citations

Keratin expression in basal cell carcinomas

1992 • 130 citations

Multiple gap junction genes are utilized during rat skin and hair development

1992 • 130 citations

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

1994 • 85 citations

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q

1996 • 66 citations

Linkage Studies of Non-Syndromic Recessive Deafness (NSRD) in a Family Originating from the Mirpur Region of Pakistan Maps DFNB1 Centromeric to D13S175

1996 • 46 citations

Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11→q12 and mouse chromosome 14D1-E1 by in situ hybridization

1996 • 33 citations

Hereditary palmoplantar keratoderma with deafness

1996 • 20 citations

Hereditary palmoplantar keratoderma with deafness

1996 • 12 citations