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Author/Creator Ahmad, Nermin

1. Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome. Issue 4 (4th June 2014)

Authors:
Al‐Haggar, Mohammad; Salem, Nanees; Wahba, Yahya; Ahmad, Nermin; Jonard, Laurence; Abdel‐Hady, Dina; El‐Hawary, Amany; El‐Sharkawy, Ashraf; Eid, Abdel‐Rhman; El‐Hawary, Amira
Journal:
Pediatric diabetes
Issue:
Volume 16:Issue 4(2015:Jul.)
Page Start:
305
Record Type:
Journal Article
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2. Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature. (14th January 2013)

Authors:
Al-Haggar, Mohammad; Ahmad, Nermin; Yahia, Sohier; Shams, Amany; Hasaneen, Bothina; Hassan Hassan, Rasha; Wahba, Yahya; Salem, Nanees Abdel-Badie; Abdel-Hady, Dina
Other Names:
Hansen T. Academic Editor.; Marquet S. Academic Editor.; Wang X. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2013(2013)
Page Start:
Record Type:
Journal Article
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