D. M. Baloch

An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group

J. Oldenburg, G. Nürnberg, P. Nürnberg, 2012, Human Genetics.

Identification of a novel mutation (p.Ile198Thr) in gene TYR in a Pakistani family with nonsyndromic oculocutaneous albinism

J. Ahmad, M. Babar, S. Daud, 2014, Clinical and experimental dermatology.

An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group

J. Oldenburg, G. Nürnberg, P. Nürnberg, 2011, Human Genetics.