Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling

Françoise Denoyelle(Centre National de la Recherche Scientifique), Sandrine Marlin(Centre National de la Recherche Scientifique), Dominique Weil(Centre National de la Recherche Scientifique), L Moatti(Hôpital Armand-Trousseau), Pierre Chauvin(Inserm), Éréa-Noël Garabédian(Hôpital Armand-Trousseau), Christine Petit(Centre National de la Recherche Scientifique)

The Lancet

April 1, 1999

10.1016/s0140-6736(98)11071-1

Cited by 437

Abstract

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