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

Prader-Willi syndrome

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

Genotype–phenotype correlation in interstitial 6q deletions: a report of 12 new cases

(2012) Jill A. Rosenfeld et al.   NEUROGENETICS

Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21)

(2010) Ana Spreiz et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Endocrine Disorders in Children with Prader-Willi Syndrome – Data from 142 Children of the French Database

(2010) G. Diene et al.   Hormone Research in Paediatrics

A de novo Proximal 6q Deletion Confirmed by Array Comparative Genomic Hybridization

(2010) Kwang-Sook Woo et al.   Korean Journal of Laboratory Medicine

Health Supervision for Children With Prader-Willi Syndrome

(2010)   PEDIATRICS

Impact of Sim1 gene dosage on the development of the paraventricular and supraoptic nuclei of the hypothalamus

(2009) Sabine Michaëlle Duplan et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype

(2008) Maria Clara Bonaglia et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Oxytocin Deficiency Mediates Hyperphagic Obesity ofSim1Haploinsufficient Mice

(2008) Bassil M. Kublaoui et al.   MOLECULAR ENDOCRINOLOGY