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Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations

✍ Scribed by Böhm, Johann; Barrionuevo, Francisco; Craig, Alexander; Unger, Sheila; Böhm, Detlef; Kaiser, Frank J; Kaulfuß, Silke; Borozdin, Wiktor; Buiting, Karin; Burfeind, Peter


Book ID
109914774
Publisher
Nature Publishing Group
Year
2008
Tongue
English
Weight
268 KB
Volume
40
Category
Article
ISSN
1061-4036

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