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A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity
Monica C. Varela, Alex Y. Simões-Sato, Chong A. Kim, Débora R. Bertola, Claudia I.E. De Castro, Celia P. KoiffmannVolume:
49
Year:
2006
Language:
english
Pages:
306
DOI:
10.1016/j.ejmg.2005.12.002
File:
PDF, 244 KB
english, 2006