Showing 1 - 5 results of 5 for search 'Ahmad Wasim', query time: 0.05s Refine Results
  1. 1
    A mutation in <it>CTSK </it>gene in an autosomal recessive pycnodysostosis family of Pakistani origin

    A mutation in <it>CTSK </it>gene in an autosomal recessive pycnodysostosis family of Pakistani origin by Ahmad Wasim, Sheikh Sabeen, Naeem Muhammad

    Published 2009
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  2. 2
    Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteaux

    Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteaux by Khan Saadullah, Ali Raja, Abbasi Sanaullah, Nawaz Muhammad, Muhammad Noor, Ahmad Wasim

    Published 2012
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  3. 3
    A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (<it>CDMP1</it>) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family

    A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (<it>CDMP1</it>) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family by Ansar Muhammad, Ali Ghazanfar, Wasif Naveed, Naqvi Syed, Basit Sulman, Ahmad Wasim

    Published 2008
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  4. 4
    Previously described sequence variant in <it>CDK5RAP2 </it>gene in a Pakistani family with autosomal recessive primary microcephaly

    Previously described sequence variant in <it>CDK5RAP2 </it>gene in a Pakistani family with autosomal recessive primary microcephaly by Hassan Muhammad, Khurshid Maryam, Azeem Zahid, John Peter, Ali Ghazanfar, Chishti Muhammad, Ahmad Wasim

    Published 2007
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  5. 5
    Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences

    Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences by Haque Sayedul, Phadke Shubha R, Roy Akhilesh K, Wajid Muhammad, Girisha KM, Malik Sajid, Ahmad Wasim, Koch Manuela C, Grzeschik Karl-Heinz

    Published 2007
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