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Springer Nature6
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✓Human Genetics6
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Syed Muhammad results 6 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Syed Muhammad ×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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Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)NARA Subscribed
Human Genetics · 2008 · Vol. 123 · Issue 5 · Springer
Zahid Azeem; Musharraf Jelani; Gul Naz; Muhammad Tariq; Naveed Wasif; Syed Kamran-ul-Hassan Naqvi; Muhammad Ayub; Masoom Yasinzai; Muhammad Amin-ud-din; Abdul Wali; Ghazanfar Ali; Muhammad Salman Chishti; Wasim Ahmad
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A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2NARA Subscribed
Human Genetics · 2008 · Vol. 123 · Issue 1 · Springer
Muhammad Jawad Hassan; Muhammad Salman Chishti; Syed Muhammad Jamal; Muhammad Tariq; Wasim Ahmad
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A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosisNARA Subscribed
Human Genetics · 2007 · Vol. 121 · Issue 3-4 · Springer
Ghazanfar Ali; Muhammad Salman Chishti; Syed Irfan Raza; Peter John; Wasim Ahmad
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Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3NARA Subscribed
Human Genetics · 2006 · Vol. 118 · Issue 5 · Springer
Peter John; Ghazanfar Ali; Muhammad S. Chishti; Syed Muhammad S. Naqvi; Suzanne M. Leal; Wasim Ahmad
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