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1 . Academic Journal
Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children.
저자
by
Eissa, Eman
;
Afifi, Hanan H.
;
Abo-Shanab, Assem M.
;
Thomas, Manal M.
;
Taher, Mohamed B.
, et al.
소스
Scientific Reports
. 9/18/2023, Vol. 13 Issue 1, p1-9. 9p.
Web of Science
Scopus
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7 . Academic Journal
Expanding the phenotypic spectrum and clinical severity associated with WLS gene
저자
by
Abdel-Salam, Ghada M. H.
;
Afifi, Hanan H.
;
Abdel-Hamid, Mohamed S.
;
Ahmed, Nermeen E. B.
;
Taher, Mohamed B.
, et al.
소스
Journal of Human Genetics
. 68(9):607-613
Web of Science
Scopus
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7 . Academic Journal
Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma.
저자
by
Eid, Ola M.
;
El Zomor, Hosam
;
Mohamed, Amal M.
;
El-Bassyouni, Hala T.
;
Afifi, Hanan H.
, et al.
소스
Ophthalmic Genetics
. Dec2022, Vol. 43 Issue 6, p789-794. 6p.
Web of Science
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7 . Academic Journal
Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.
저자
by
Afifi, Hanan H.
;
Gaber, Khaled R.
;
Thomas, Manal M.
;
Taher, Mohamed B.
;
Tosson, Angie M.S.
.
소스
American Journal of Perinatology
. Nov2022, Vol. 39 Issue 15, p1659-1667. 9p.
Web of Science
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7 . Academic Journal
Further Evidence of a Continuum in the Clinical Spectrum of Dominant PIEZO2-Related Disorders and Implications in Cerebellar Anomalies.
저자
by
Abdel-Salam, Ghada M.H.
;
Afifi, Hanan H.
;
Saleem, Sahar N.
;
Gadelhak, Mohamed I.
;
El-Serafy, Manar A.
, et al.
소스
Molecular Syndromology; 2022, Vol. 13 Issue 5, p389-396, 8p
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7 . Academic Journal
Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.
저자
by
Mohamed, Amal M.
;
Kamel, Alaa K.
;
Eid, Maha M.
;
Eid, Ola M.
;
Mekkawy, Mona
, et al.
소스
Molecular Genetics & Genomic Medicine
. Nov2021, Vol. 9 Issue 11, p1-15. 15p.
Open Access (Wiley)
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7 . Periodical
Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant
저자
by
Afifi, Hanan H.
;
El-Kamah, Ghada Y.
;
Kamel, Alaa K.
;
Abd Allah, Sally G.
;
Hammad, Sayda
, et al.
소스
Journal of Pediatric Genetics; June 2021, Vol. 10 Issue: 2 p131-138, 8p
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7 . Academic Journal
Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.
저자
by
Abdel‐Salam, Ghada M. H.
;
Sayed, Inas S. M.
;
Afifi, Hanan H.
;
Abdel‐Ghafar, Sherif F.
;
Abouzaid, Maha R.
, et al.
소스
American Journal of Medical Genetics. Part A; Jun2020, Vol. 182 Issue 6, p1407-1420, 14p
Web of Science
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7 . Academic Journal
Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomalies.
저자
by
Mohammad, Shaimaa Abdelsattar
;
Abdelaziz, Tougan Taha
;
Gadelhak, Mohamed I.
;
Afifi, Hanan H.
;
Abdel-Salam, Ghada M. H.
.
소스
Neuroradiology
(NEURORADIOLOGY), Oct2018; 60(10): 1053-1061. (9p)
EBSCOHost PDF
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7 . Academic Journal
Lenz–Majewski syndrome in a patient from Egypt.
저자
by
Afifi, Hanan H.
;
Abdel‐Hamid, Mohamed S.
;
Mehrez, Mennat I.
;
El‐Kamah, Ghada
;
Abdel‐Salam, Ghada M. H.
.
소스
American Journal of Medical Genetics. Part A; Oct2019, Vol. 179 Issue 10, p2039-2042, 4p
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