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Immunologic compensation in a patient with a large IgH constant region deletion

✍ Scribed by Depiero, Andrew; Kaminski, Denise A.; Halsey, John F.; Briles, David; Burrows, Peter D.; Hostoffer, Robert W.


Book ID
119765274
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
193 KB
Volume
107
Category
Article
ISSN
1097-6825

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Fragile X phenotype in a patient with a
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## Abstract A 2‐year‐old boy with manifestations of the fragile X syndrome was found to have a cytogenetically visible deletion of Xq27‐q28 including deletion of FMR‐1. Molecular analysis of the patient was recently described in Tarleton et al. [1993: Hum Mol Genet 2(11): 1973–1974] and the deletio