Detalhe da pesquisa
1.
Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation.
Cytogenet Genome Res
; 160(3): 124-133, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32187602
2.
Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features.
Cytogenet Genome Res
; 159(3): 130-136, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31715598
3.
Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome.
Am J Med Genet A
; 170(10): 2662-70, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27264538
4.
Effect of Soybean Oil on the Improvement of the Functionality of Edible Membrane-Type Food Packaging Films Based on Caseinate-Carboxymethyl Chitosan Compositions.
Membranes (Basel)
; 14(5)2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38786938
5.
An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization.
J Assist Reprod Genet
; 35(8): 1503-1508, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29860576
6.
Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients.
J Genet Eng Biotechnol
; 21(1): 149, 2023 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38017244
7.
Expansion of the phenotypic and mutational spectrum of Carpenter syndrome.
Eur J Med Genet
; 65(1): 104377, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34748996
8.
Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma.
Ophthalmic Genet
; 43(6): 789-794, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36098066
9.
Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant.
J Pediatr Genet
; 10(2): 131-138, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33996184
10.
Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.
Mol Genet Genomic Med
; 9(2): e1546, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33217222
11.
Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.
Mol Genet Genomic Med
; 9(11): e1829, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34609792
12.
Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt.
Am J Trop Med Hyg
; 102(4): 719-723, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32124726
13.
Cyclin D1 gene amplification in proliferating haemangioma.
Cell Tissue Res
; 338(1): 107-15, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19823825
14.
Predictors of MERS-CoV infection: A large case control study of patients presenting with ILI at a MERS-CoV referral hospital in Saudi Arabia.
Travel Med Infect Dis
; 14(5): 464-470, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27671972
15.
Isolation and Molecular Characterization of Mycoplasma gallisepticum and Mycoplasma synoviae in Chickens in Sudan.
J Vet Med
; 2013: 208026, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-26464902