The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families

Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis

(2015) Dan Mejlachowicz et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Autism spectrum disorder in Prader-Willi syndrome: A systematic review

(2015) Jeffrey A. Bennett et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism

(2015) Hamid Meziane et al.   BIOLOGICAL PSYCHIATRY

MAGEL2 and Oxytocin—Implications in Prader-Willi Syndrome and Beyond

(2015) Michael D. Fountain et al.   BIOLOGICAL PSYCHIATRY

Clinical phenotypes of MAGEL2 mutations and deletions

(2014) Karin Buiting et al.   Orphanet Journal of Rare Diseases

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

(2014) S. E. Soden et al.   Science Translational Medicine

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

(2013) Christian P Schaaf et al.   NATURE GENETICS

Nutritional phases in Prader-Willi syndrome

(2011) Jennifer L. Miller et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Variations in fetal phenotype in Prader-Willi syndrome

(2009) Guttorm Haugen et al.   PRENATAL DIAGNOSIS

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

(2008) Deniz Kanber et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Prader-Willi syndrome: is there a recognizable fetal phenotype?

(2008) Nicole Bigi et al.   PRENATAL DIAGNOSIS