Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly

Por Hassan, Muhammad Jawad, Khurshid, Maryam, Azeem, Zahid, John, Peter, Ali, Ghazanfar, Chishti, Muhammad Salman, Ahmad, Wasim
Publicado em 2007

Hyperventilation-athetosis in ASXL3 deficiency (Bainbridge-Ropers) syndrome

Por Dad, Rubina, Walker, Susan, Scherer, Stephen W., Hassan, Muhammad Jawad, Kang, Suk Yun, Minassian, Berge A.
Publicado no Neurol Genet (2017)

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

Por Kousar, Rizwana, Hassan, Muhammad Jawad, Khan, Bushra, Basit, Sulman, Mahmood, Saqib, Mir, Asif, Ahmad, Wasim, Ansar, Muhammad
Publicado em 2011

Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3

Por Chishti, Muhammad Salman, Lee, Kwanghyuk, McDonald, Merry-Lynn, Hassan, Muhammad Jawad, Ansar, Muhammad, Ahmad, Wasim, Leal, Suzanne M
Publicado em 2009

Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2–q13.32

Por Tariq, Aamira, Santos, Regie Lyn P., Khan, Mohammad Nasim, Lee, Kwanghyuk, Hassan, Muhammad Jawad, Ahmad, Wasim, Leal, Suzanne M.
Publicado em 2006

Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype

Por Dad, Rubina, Walker, Susan, Scherer, Stephen W., Hassan, Muhammad Jawad, Alghamdi, Mohammad Domaia, Minassian, Berge A., Alkhater, Reem A.
Publicado no Neurol Genet (2017)

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2

Por Santos, Regie Lyn P., Hassan, Muhammad Jawad, Sikandar, Shaheen, Lee, Kwanghyuk, Ali, Ghazanfar, Martin, Protacio E., Wambangco, Michael Angelo L., Ahmad, Wasim, Leal, Suzanne M.
Publicado em 2006

A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3

Por Hassan, Muhammad Jawad, Santos, Regie Lyn P., Rafiq, Muhammad Arshad, Chahrour, Maria H., Pham, Thanh L., Wajid, Muhammad, Hijab, Nadine, Wambangco, Michael, Lee, Kwanghyuk, Ansar, Muhammad, Yan, Kai, Ahmad, Wasim, Leal, Suzanne M.
Publicado em 2005

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

Por Santos-Cortez, Regie Lyn P., Faridi, Rabia, Rehman, Atteeq U., Lee, Kwanghyuk, Ansar, Muhammad, Wang, Xin, Morell, Robert J., Isaacson, Rivka, Belyantseva, Inna A., Dai, Hang, Acharya, Anushree, Qaiser, Tanveer A., Muhammad, Dost, Ali, Rana Amjad, Shams, Sulaiman, Hassan, Muhammad Jawad, Shahzad, Shaheen, Raza, Syed Irfan, Bashir, Zil-e-Huma, Smith, Joshua D., Nickerson, Deborah A., Bamshad, Michael J., Riazuddin, Sheikh, Ahmad, Wasim, Friedman, Thomas B., Leal, Suzanne M.
Publicado no Am J Hum Genet (2016)