𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Familial partial epilepsy with variable foci: A new family with suggestion of linkage to chromosome 22q12

✍ Scribed by José Morales-Corraliza; Pilar Gómez-Garre; Raúl Sanz; Fernando Díaz-Otero; Eva Gutiérrez-Delicado; José M. Serratosa


Book ID
109112805
Publisher
Wiley (Blackwell Publishing)
Year
2010
Tongue
English
Weight
607 KB
Volume
51
Category
Article
ISSN
0013-9580

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


FG syndrome: Report of three new familie
✍ Graham, John M.; Tackels, Darci; Dibbern, Kurt; Superneau, Duane; Rogers, Curtis 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 70 KB 👁 2 views

FG syndrome is a rare X-linked recessive form of mental retardation, first described by Opitz and Kaveggia in 1974 in five related males with mental retardation, disproportionately large heads, imperforate anus, and congenital hypotonia. Partial agenesis of the corpus callosum was noted in at least