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A Turner syndrome neurocognitive phenotype maps to Xp22.3

✍ Scribed by Andrew R Zinn; David Roeltgen; Gerry Stefanatos; Purita Ramos; Frederick F Elder; Harvey Kushner; Karen Kowal; Judith L Ross


Book ID
119909289
Publisher
BioMed Central
Year
2007
Tongue
English
Weight
674 KB
Volume
3
Category
Article
ISSN
1744-9081

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## Abstract Coffin‐Lowry syndrome (CLS; MIM 303600) is an uncommon X‐linked disorder causing mental retardation and skeletal abnormalities. Most recently it was mapped to a 5.6‐centimorgan (cM) region of Xp22, flanked distally by AFM291 wf5 and proximally by DXS1052 [Biancalana et al., 1994: Genomi