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Characterization ofSCML1,a New Gene in Xp22, with Homology to Developmental Polycomb Genes

✍ Scribed by Esther van de Vosse; Susannah M. Walpole; Alexia Nicolaou; Paola van der Bent; Anthony Cahn; Mark Vaudin; Mark T. Ross; Jillian Durham; Rebecca Pavitt; Jane Wilkinson; Darren Grafham; Arthur A.B. Bergen; Gert-Jan B. van Ommen; John R.W. Yates; Johan T. den Dunnen; Dorothy Trump


Book ID
115614257
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
256 KB
Volume
49
Category
Article
ISSN
0888-7543

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X-linked mental retardation with neonata
✍ Raynaud, Martine; Gendrot, Chantal; Dessay, Benoit; Moncla, Anne; Ayrault, Anne- πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 860 KB

Linkage analysis was performed in a family with non-specific X-linked mental retardation (MRX 15). Hypotonia in infancy was the most remarkable physical manifestation. The severity of mental deficiency was variable among the patients, but all of them had poor or absent speech. Significant lod scores