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 - Concepedia

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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

122

Citations

17

References

2006

Year

Carla S. D’Angelo, José Albino da Paz, Chong Ae Kim, Débora Romeo Bertola, Cláudia Irene Emílio de Castro, Monica Castro Varela, Célia Priszkulnik Koiffmann

European Journal of Medical Genetics

PsychiatryGenetic DisorderMedicineBehavioral ProblemsNeuropsychiatryNeurologyBiological PsychiatryPrader-willi-like PhenotypeDelayed Psychomotor DevelopmentNeurogenetics

References

	Year	Citations

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