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Springer Nature4
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✓Human Genetics4
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20121
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Muhammad Basit results 4 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Muhammad Basit ×Clear All Filters
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Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genesNARA Subscribed
Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer
Umm-e-Kalsoom; Sulman Basit; Syed Kamran-ul-Hassan Naqvi; Muhammad Ansar; Wasim Ahmad
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Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani familiesNARA Subscribed
Human Genetics · 2011 · Vol. 129 · Issue 4 · Springer
Naveed Wasif; Syed Kamran ul-Hassan Naqvi; Sulman Basit; Nadir Ali; Muhammad Ansar; Wasim Ahmad
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DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2NARA Subscribed
Human Genetics · 2011 · Vol. 129 · Issue 4 · Springer
Sulman Basit; Kwanghyuk Lee; Rabia Habib; Leon Chen; Umm-e-Kalsoom; Regie Lyn P. Santos-Cortez; Zahid Azeem; Paula Andrade; Muhammad Ansar; Wasim Ahmad; Suzanne M. Leal
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Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genesNARA Subscribed
Human Genetics · 2010 · Vol. 128 · Issue 2 · Springer
Sulman Basit; Ghazanfar Ali; Naveed Wasif; Muhammad Ansar; Wasim Ahmad
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