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2006•European Journal of Medical GeneticsRequires access

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 Albino da Paz, Chong Ae Kim, Débora Romeo Bertola, Cláudia Irene Emílio de Castro, Monica Castro Varela, Célia Priszkulnik Koiffmann

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Key concepts: Hypotonia, Monosomy, Microcephaly, Chromosomal Deletion, Genetics, Biology, Subtelomere, Psychomotor disorder

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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 — Research Paper | ScholarLens