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Overgrowth of a Mouse Model of the Simpson–Golabi–Behmel Syndrome Is Independent of IGF Signaling

✍ Scribed by Eric Chiao; Peter Fisher; Laura Crisponi; Manila Deiana; Ioannis Dragatsis; David Schlessinger; Giuseppe Pilia; Argiris Efstratiadis

Book ID
115598920
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
540 KB
Volume
243
Category
Article
ISSN
0012-1606

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GPC3 mutation analysis in a spectrum of
GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome
✍ Li, Madeline ;Shuman, Cheryl ;Fei, Yan Ling ;Cutiongco, Eva ;Bender, H.A. ;Steve 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 283 KB 👁 2 views

Simpson-Golabi-Behmel syndrome (SGBS) is an X-linked overgrowth syndrome caused by deletions in glypican 3 (GPC3). SGBS is characterized by pre- and postnatal overgrowth, a characteristic facial appearance, and a spectrum of congenital malformations which overlaps that of other overgrowth syndromes.