Phenotypic heterogeneity in Woodhouse-Sakati syndrome: Two new families with a mutation in the C2orf37 gene

Woodhouse-Sakati Syndrome in an Israeli-Arab Family Presenting with Youth-Onset Diabetes Mellitus and Delayed Puberty

(2011) Marianna Rachmiel et al.   Hormone Research in Paediatrics

A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome

(2010) K Steindl et al.   CLINICAL GENETICS

C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients

(2010) AM Alazami et al.   CLINICAL GENETICS

Allelic heterogeneity in inbred populations: The Saudi experience with Alström syndrome as an illustrative example

(2009) Mohamed A. Aldahmesh et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Three siblings with Woodhouse–Sakati syndrome in an Indian family

(2009) George Koshy et al.   CLINICAL DYSMORPHOLOGY

Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

(2008) Anas M. Alazami et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Dystonia in the Woodhouse Sakati syndrome: A new family and literature review

(2008) Susanne A. Schneider et al.   MOVEMENT DISORDERS