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Terminal deletion of 6q and Fryns syndrome: A microdeletion/syndrome pair?

✍ Scribed by Krassikoff, Natalie ;Sekhon, Gurbax S.


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
236 KB
Volume
36
Category
Article
ISSN
0148-7299

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We report on an 8-year-old boy with a proximal interstitial deletion of the long arm of chromosome 6 with breakpoints q13 to q14.2. He has a characteristic facial appearance that is seen in several of the previously described cases. Details of his clinical course are reviewed and compared with the n