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A case report of 46, XX, del (21)(q22) de novo deletion associated with Imerslund-Grasbeck syndrome

✍ Scribed by Figen Celep; Ahmet Karagüzel; F. Müjgan Aynaci; Erol Erduran


Book ID
115091842
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
288 KB
Volume
50
Category
Article
ISSN
0009-9163

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## Abstract Mosaicism for two chromosomally abnormal cell lines in the absence of a normal cell line is exceedingly rare. We report a patient with developmental and growth delay, mild dysmorphic features, a history of hypertension and hepatoblastoma who was found to be mosaic for two chromosomally