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                                       Details for article 8 of 17 found articles
 
 
  Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
 
 
Title: Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
Author: Alazami, Anas M.
Al-Saif, Amr
Al-Semari, Abdulaziz
Bohlega, Saeed
Zlitni, Soumaya
Alzahrani, Fatema
Bavi, Prashant
Kaya, Namik
Colak, Dilek
Khalak, Hanif
Baltus, Andy
Peterlin, Borut
Danda, Sumita
Bhatia, Kailash P.
Schneider, Susanne A.
Sakati, Nadia
Walsh, Christopher A.
Al-Mohanna, Futwan
Meyer, Brian
Alkuraya, Fowzan S.
Appeared in: The American journal of human genetics
Paging: Volume 83 (2008) nr. 6 pages 8 p.
Year: 2008
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 8 of 17 found articles
 
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