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Ibtisam M. Hammad

Observed names: I Hammad, I.M. Hammad
OpenAlex ID: A5111699642
Familial Manic–Depressive Illness with Deleted Short Arm of Chromosome 21: Coincidental or Causal?
1989 · Magda H. El-Badramany, Talaat I. Farag, et al. · The British Journal of Psychiatry · 12
Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.
1993 · F M Mohammed, D S Krishna Murthy, et al. · PubMed · 4
Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature.
1990 · S J Abulhasan, A S Teebi, et al. · PubMed · 2
Mental Retardation and Phenotypic Abnormalities Associated with Apparently Balanced Translocation Involving Chromosomes 2, 3 and 7
2008 · T.S. Sundareshan, M.Y. El-Khalifa, et al. · Medical Principles and Practice · 1
Works count: 4
Citation count: 19
H-index: 2
I10-index: 1
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