Haque S

Publications (2)0 Total impact

• Article: A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.

  Rafiq MA, Ansar M, Mahmood S, Haque S, Faiyaz-ul-Haque M, Leal SM, Ahmad W.
  J Invest Dermatol. 07/2004; 123(1):247-8.
• Article: A locus for hereditary hypotrychosis localized to human chromosome 18q21.1

  Rafique MA, Ansar M, Jamal SM, Malik S, Sohail M, Faiyaz-Ul-Haque M, Haque S, Leal SM, Ahmad W
  European Journal of Human Genetics, 2003,. 01/2003; 11:623-628.