𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A girl with G syndrome and agenesis of the corpus callosum

✍ Scribed by Neri, G. ;Genuardi, M. ;Natoli, G. ;Costa, P. ;Maggioni, G. ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
260 KB
Volume
28
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Pai syndrome: First patient with agenesi
✍ Marco Castori; Rosanna Rinaldi; Aurelia Bianchi; Aurelio Caponetti; Marcello Ass πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 178 KB πŸ‘ 1 views

## Abstract ## BACKGROUND: Pai syndrome (PS) is a rare regional developmental defect of the face, mainly characterized by the variable association of midline cleft of the upper lip (MCL), duplicated maxillary median frenulum, and midline facial cutaneous and midanterior alveolar process polyps. It

Agenesis of the corpus callosum in a mot
✍ Inbar, Dov; Halpern, Gabrielle J.; Weitz, Raphael; Sadeh, Michelle; Shohat, Mord πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 162 KB πŸ‘ 2 views

Most reported familial cases of agenesis of the corpus callosum have followed either an autosomal recessive or an X-linked recessive pattern of inheritance. To the best of our knowledge, there is only one previous report of a family showing clear-cut autosomal dominant inheritance. We present the se