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Wasim Ahmad
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Journal Articles

Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3

Subject Area:
Genetics
Ghazanfar Ali, Kwanghyuk Lee, Paula B. Andrade, Sulman Basit, Regie Lyn P. Santos-Cortez, Leon Chen, Musharraf Jelani, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal
Journal: Human Heredity
Hum Hered (2011) 71 (2): 106–112.
https://doi.org/10.1159/000320154
Published Online: 06 July 2011
View article titled, Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3
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Journal Articles

DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22

Subject Area:
Genetics
Muhammad Ansar, Maria H. Chahrour, Mohammad Amin ud Din, Muhammad Arshad, Sayedul Haque, Thanh L. Pham, Kai Yan, Wasim Ahmad, Suzanne M. Leal
Journal: Human Heredity
Hum Hered (2004) 57 (4): 195–199.
https://doi.org/10.1159/000081446
Published Online: 26 November 2004
View article titled, DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22
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Journal Articles

Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26-q27 in a Consanguineous Kindred from Pakistan

Subject Area:
Genetics
Muhammad Ansar, Mohammad Ramzan, Thanh L. Pham, Kai Yan, Syed Muhammad Jamal, Sayedul Haque, Wasim Ahmad, Suzanne M. Leal
Journal: Human Heredity
Hum Hered (2003) 55 (1): 71–74.
https://doi.org/10.1159/000071813
Published Online: 06 August 2003
View article titled, Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26-q27 in a Consanguineous Kindred from Pakistan
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Journal Articles

Identification of a Founder Mutation in the Protoporphyrinogen Oxidase Gene in Variegate Porphyria Patients from Chile

Subject Area:
Genetics
Jorge Frank, Vincent M. Aita, Wasim Ahmad, HaMut Lam, Carlos Wolff, Angela M. Christiano
Journal: Human Heredity
Hum Hered (2001) 51 (3): 160–168.
https://doi.org/10.1159/000053337
Published Online: 25 January 2001
View article titled, Identification of a Founder Mutation in the Protoporphyrinogen Oxidase Gene in Variegate Porphyria Patients from Chile
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