Search Results - "Kayed, H F"

Holoprosencephaly spectrum among Egyptian patients: clinical and cytogenetic study by El-Bassyouni, H T, Abdel Salam, G H, Saleem, S N, Kayed, H F, Shehab, M I, Eid, M M, Zaki, M E, Zaki, M S

“…We report 24 patients with holoprosencephaly (HPE) spectrum screened for Del 7q36 and subtelomere 13q. They were divided according to the type of HPE into: 6…”
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Phenotypic variability in Micro syndrome: report of new cases by Abdel-Salam, G M H, Hassan, N A, Kayed, H F, Aligianis, I A

“…The authors describe seven Egyptian patients (5 males and two females) with microcephaly, mild microphthalmia, microcornea, congenital cataracts and…”
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Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics by Afifi, H H, Zaki, M S, El-Gerzawy, A M S, Kayed, H F

“…Jacobsen syndrome is a rare disorder, caused by segmental monosomy for the distal end of the long arm of chromosome 11 with variable phenotypic expressivity…”
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Screening for chromosomal abnormalities in 2650 infertile couples undergoing ICSI by Kayed, Hesham F, Mansour, Ragaa T, Aboulghar, Mohamed A, Serour, Gamal I, Amer, Alaa E, Abdrazik, Ashraf

“…Chromosomal abnormalities are the major contributor to the genetic risks of infertility treatment associated with intracytoplasmic sperm injection (ICSI). The…”
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