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

✍ Scribed by Francoise Denoyelle; Sandrine Marlin; Dominique Weil; Lucien Moatti; Pierre Chauvin; Éréa-Noël Garabédian; Christine Petit


Book ID
117311696
Publisher
The Lancet
Year
1999
Tongue
English
Weight
132 KB
Volume
353
Category
Article
ISSN
0140-6736

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