𝔖 Bobbio Scriptorium
✦   LIBER   ✦

FMR1 and the fragile X syndrome: Human genome epidemiology review

✍ Scribed by Crawford, Dana C; Acuña, Juan M; Sherman, Stephanie L


Book ID
121864397
Publisher
Nature Publishing Group
Year
2001
Tongue
English
Weight
125 KB
Volume
3
Category
Article
ISSN
1098-3600

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


FMR1 gene and fragile X syndrome
✍ Bardoni, Barbara ;Mandel, Jean-Louis ;Fisch, Gene S. 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 187 KB 👁 2 views

Taxonomic features of fragile X syndrome (FXS) associated with the fragile X mutation have evolved over several decades. Males are more severely impacted cognitively than females, but both show declines in IQ scores as they age. Although many males with FXS exhibit autistic-like features, autism doe

Fragile X syndrome and deletions in FMR1
✍ Hammond, Lyn S.; Macias, Michelle M.; Tarleton, Jack C.; Pai, G. Shashidhar 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB 👁 2 views

The fragile X syndrome phenotype of mental retardation is almost always caused by abnormal CGG trinucleotide amplification within the FMR1 gene. Occasionally fragile X syndrome results from point mutations or deletions within or around the FMR1 locus. We have identified a mentally retarded African A