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NARA Subscribed2
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Springer Nature2
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✓Human Genetics2
Publication Year
20191
20061
H. Muhammad results 2 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: H. Muhammad ×Clear All Filters
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GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimatesNARA Subscribed
Human Genetics · 2019 · Vol. 138 · Issue 10 · Springer
Qing Ouyang; Brian C. Kavanaugh; Lena Joesch-Cohen; Bethany Dubois; Qing Wu; Michael Schmidt; Ozan Baytas; Stephen F. Pastore; Ricardo Harripaul; Sasmita Mishra; Abrar Hussain; Katherine H. Kim; Yolanda F. Holler-Managan; Muhammad Ayub; Asif Mir; John B. Vincent; Judy S. Liu; Eric M. Morrow
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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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