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Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented

✍ Scribed by Eve Õiglane-Shlik; Tiina Talvik; Riina Žordania; Haide Põder; Tiina Kahre; Elve Raukas; Tiiu Ilus; Gunnar Tasa; Oliver Bartsch; Marja-Leena Väisänen; Katrin Õunap

Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
123 KB
Volume
140A
Category
Article
ISSN
1552-4825

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FISH detection of chromosome 15 deletion
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✍ Teshima, I.; Chadwick, D.; Chitayat, D.; Kobayashi, J.; Ray, P.; Shuman, C.; Sie 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 51 KB 👁 2 views

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