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Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies

✍ Scribed by Lucilene Arilho Ribeiro-Bicudo; Rodrigo G. Quiezi; Maria Leine Guion-Almeida; Chiara Legnaro; Antonio Richieri-Costa


Book ID
111995142
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
119 KB
Volume
158A
Category
Article
ISSN
1552-4825

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