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Unilateral focal polymicrogyria in a patient with classical Aarskog–Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1

✍ Scribed by Armand Bottani; Alfredo Orrico; Lucia Galli; Olivier Karam; Charles-André Haenggeli; Solène Ferey; Bernard Conrad


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
224 KB
Volume
143A
Category
Article
ISSN
1552-4825

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