6q16.3q23.3 duplication associated with Prader-Willi-like syndrome

New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity

(2014) Marie-Laure Vuillaume et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1

(2014) Laïla El Khattabi et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mini-Review Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities

(2014) C.F. Rocha et al.   GENETICS AND MOLECULAR RESEARCH

Endocrine phenotype of 6q16.1-q21 deletion involvingSIM1and Prader-Willi syndrome-like features

(2013) Kosuke Izumi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants

(2013) Carla Sustek D'Angelo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Molecular characterization of 39de novosSMC: contribution to prognosis and genetic counselling, a prospective study

(2013) N. Marle et al.   CLINICAL GENETICS

Complex small supernumerary marker chromosomes – an update

(2013) Thomas Liehr et al.   Molecular Cytogenetics

Supernumerary marker chromosomes derived from chromosome 6: Cytogenetic, molecular cytogenetic, and array CGH characterization

(2012) Bing Huang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prader-Willi syndrome

(2012) Suzanne B. Cassidy et al.   GENETICS IN MEDICINE

Prader–Willi syndrome

(2008) Suzanne B Cassidy et al.   EUROPEAN JOURNAL OF HUMAN GENETICS