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Fragile X syndrome and 22q11.2 microdeletion in the same sibship

✍ Scribed by Missirian, Chantal ;Moncla, Anne ;Voelckel, Marie-Antoinette ;Ravix, Val�ry ;Philip, Nicole

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
195 KB
Volume
95
Category
Article
ISSN
0148-7299

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Letter to the Editor ## Opitz GBBB Syndrome and the 22q11.2 Deletion To the Editor: Recently, McDonald-McGinn et al. [1995] reported the presence of a deletion 22q11.2 in a family with autosomal dominant inheritance and in a sporadic case with the Opitz GBBB syndrome.The presence of a vascular r