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Research Paper Detail

A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1

Publisher: Gene
Publication Year: 2014

First Author:  Agha, Z Second Author:  Iqbal, Z
Third Author:  Raheel Qamar Volume:  538
Publication #:  Page #:  30-35
Level:   International Type:  Journal
Email:  raheel_qamar@comsats.edu.pk
Prof. Dr. Raheel Qamar, T.I.

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