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Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations

✍ Scribed by Delezoide, A.L.; Vekemans, M.

Book ID: 122618642
Publisher: Elsevier Science
Year: 1994
Tongue: English
Weight: 446 KB
Volume: 48
Category: Article
ISSN: 0753-3322
DOI: 10.1016/0753-3322(94)90047-7

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