Prader-Willi-Like phenotype investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems

Carla Sustek D'Angelo José A. da Paz; Chong A Kim; Débora R Bertola; Cláudia Irene Emílio de Castro; Monica Castro Varela; Célia Priszkulnik Koiffmann; Annual Meeting of the American Society of Human Genetics (55. 2005 Salt Lake City, Utah, EUA)

Abstracts Salt Lake City, 2005

Salt Lake City 2005

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