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Fluorescent in situ hybridization for evaluation of prader-willi and angelman syndromes

โœ Scribed by Wenger, Sharon L. ;Cummins, James H.


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
91 KB
Volume
57
Category
Article
ISSN
0148-7299

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We have evaluated fluorescence in situ hybridization (FISH) analysis for the clinical laboratory detection of the 15qll-ql3 deletion seen in Prader-Willi syndrome (PWS) and Angelman syndrome (AS) using probes for loci D15Sl1, SNRPN, D15S10, and GABRB3. In a series of 118 samples from patients referr