Published in
Elsevier, European Journal of Medical Genetics, 12(60), p. 627-630
DOI: 10.1016/j.ejmg.2017.07.017
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A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family
Journal article published in 2017 by
Uzma Abdullah,
Muhammad Farooq,
Yuan Mang,
Syeda Marriam Bakhtiar,
Ambrin Fatima,
Lars Hansen,
Klaus Wilbrandt Kjaer,
Lars Allan Larsen 
,
Sanam Faryal,
Niels Tommerup ,
Shahid Mahmood Baig
,
Sanam Faryal,
Niels Tommerup ,
Shahid Mahmood Baig
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