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Springer Nature14
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✓Human Genetics14
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Muhammad Wasim results 14 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Muhammad Wasim ×Clear All Filters
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Variants in KIAA0825 underlie autosomal recessive postaxial polydactylyNARA Subscribed
Human Genetics · 2019 · Vol. 138 · Issue 6 · Springer
Irfan Ullah; Naseebullah Kakar; Isabelle Schrauwen; Shabir Hussain; Imen Chakchouk; Khurram Liaqat; Anushree Acharya; Naveed Wasif; Regie Lyn P. Santos-Cortez; Saadullah Khan; Abdul Aziz; Kwanghyuk Lee; Julien Couthouis; Denise Horn; Bjørt K. Kragesteen; Malte Spielmann; Holger Thiele; Deborah A. Nickerson; Michael J. Bamshad; Aaron D. Gitler; Jamil Ahmad; Muhammad Ansar; Guntram Borck; Wasim Ahmad; Suzanne M. Leal
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Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disabilityNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 9 · Springer
Regie Lyn P. Santos-Cortez; Valeed Khan; Falak Sher Khan; Zaib-un-Nisa Mughal; Imen Chakchouk; Kwanghyuk Lee; Memoona Rasheed; Rifat Hamza; Anushree Acharya; Ehsan Ullah; Muhammad Arif Nadeem Saqib; Izoduwa Abbe; Ghazanfar Ali; Muhammad Jawad Hassan; Saadullah Khan; Zahid Azeem; Irfan Ullah; Michael J. Bamshad; Deborah A. Nickerson; Isabelle Schrauwen; Wasim Ahmad; Muhammad Ansar; Suzanne M. Leal
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Mutation of ATF6 causes autosomal recessive achromatopsiaNARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 9 · Springer
Muhammad Ansar; Regie Lyn P. Santos-Cortez; Muhammad Arif Nadeem Saqib; Fareeha Zulfiqar; Kwanghyuk Lee; Naeem Mahmood Ashraf; Ehsan Ullah; Xin Wang; Sundus Sajid; Falak Sher Khan; Muhammad Amin-ud-Din; Joshua D. Smith; Jay Shendure; Michael J. Bamshad; Deborah A. Nickerson; Abdul Hameed; Saima Riazuddin; Zubair M. Ahmed; Wasim Ahmad; Suzanne M. Leal
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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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Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3NARA Subscribed
Human Genetics · 2009 · Vol. 125 · Issue 4 · Springer
Muhammad Tariq; Muhammad Nasim Khan; 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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DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2NARA Subscribed
Human Genetics · 2006 · Vol. 120 · Issue 1 · Springer
Regie Lyn P. Santos; Muhammad Jawad Hassan; Shaheen Sikandar; Kwanghyuk Lee; Ghazanfar Ali; Protacio E. Martin; Michael Angelo L. Wambangco; Wasim Ahmad; Suzanne M. Leal
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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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A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3NARA Subscribed
Human Genetics · 2006 · Vol. 118 · Issue 5 · Springer
Muhammad Jawad Hassan; Regie Lyn P. Santos; Muhammad Arshad Rafiq; Maria H. Chahrour; Thanh L. Pham; Muhammad Wajid; Nadine Hijab; Michael Wambangco; Kwanghyuk Lee; Muhammad Ansar; Kai Yan; Wasim Ahmad; Suzanne M. Leal
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