Search Results - "Hussen DF"

Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants.

Authors: Elaraby NM Metwally AM Sayed SM et al.

Source: Molecular and cellular pediatrics [Mol Cell Pediatr] 2025 Nov 25; Vol. 12 (1), pp. 22. Date of Electronic Publication: 2025 Nov 25.

Publication Type: Journal Article

Journal Info: Publisher: Springer Country of Publication: Germany NLM ID: 101660689 Publication Model: Electronic Cited Medium: Print ISSN: 2194-7791 (Print) Linking ISSN: 21947791 NLM ISO Abbreviation: Mol Cell Pediatr Subsets: PubMed not MEDLINE

Biallelic TYR and TKFC variants in Egyptian patients with OCA1 and new expanded TKFC features.

Authors: Ashaat EA Esmaiel NN El-Saiedi SA et al.

Source: BMC genomics [BMC Genomics] 2024 Sep 09; Vol. 25 (1), pp. 844. Date of Electronic Publication: 2024 Sep 09.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 100965258 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2164 (Electronic) Linking ISSN: 14712164 NLM ISO Abbreviation: BMC Genomics Subsets: MEDLINE

The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy.

Authors: Ashaat EA Ahmed HA Elaraby NM et al.

Source: Molecular neurobiology [Mol Neurobiol] 2024 Aug; Vol. 61 (8), pp. 4949-4961. Date of Electronic Publication: 2023 Dec 28.

Publication Type: Journal Article

Journal Info: Publisher: Humana Press Country of Publication: United States NLM ID: 8900963 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1559-1182 (Electronic) Linking ISSN: 08937648 NLM ISO Abbreviation: Mol Neurobiol Subsets: MEDLINE

Rubinstein-Taybi syndrome in diverse populations.

Authors: Tekendo-Ngongang C Owosela B Fleischer N et al.

Source: American journal of medical genetics. Part A [Am J Med Genet A] 2020 Dec; Vol. 182 (12), pp. 2939-2950. Date of Electronic Publication: 2020 Sep 27.

Publication Type: Journal Article; Research Support, N.I.H., Intramural

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.

Authors: Hussen DF Kamel AK Mekkawy MK et al.

Source: Molecular syndromology [Mol Syndromol] 2020 Dec; Vol. 11 (5-6), pp. 284-295. Date of Electronic Publication: 2020 Sep 23.

Publication Type: Journal Article

Journal Info: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

Turner syndrome in diverse populations.

Authors: Kruszka P Addissie YA Tekendo-Ngongang C et al.

Source: American journal of medical genetics. Part A [Am J Med Genet A] 2020 Feb; Vol. 182 (2), pp. 303-313. Date of Electronic Publication: 2019 Dec 19.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Williams-Beuren syndrome in diverse populations.

Authors: Kruszka P Porras AR de Souza DH et al.

Source: American journal of medical genetics. Part A [Am J Med Genet A] 2018 May; Vol. 176 (5), pp. 1128-1136.

Publication Type: Journal Article; Meta-Analysis; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

The Micronuclei Scoring as a Biomarker for Early Detection of Genotoxic Effect of Cigarette Smoking.

Authors: Mohammed AM Hussen DF Rashad H et al.

Source: Asian Pacific journal of cancer prevention : APJCP [Asian Pac J Cancer Prev] 2020 Jan 01; Vol. 21 (1), pp. 87-92. Date of Electronic Publication: 2020 Jan 01.

Publication Type: Journal Article

Journal Info: Publisher: Asian Pacific Organization for Cancer Prevention Country of Publication: Thailand NLM ID: 101130625 Publication Model: Electronic Cited Medium: Internet ISSN: 2476-762X (Electronic) Linking ISSN: 15137368 NLM ISO Abbreviation: Asian Pac J Cancer Prev Subsets: MEDLINE

Genetics and Genomic Medicine in Egypt: steady pace.

Authors: Temtamy SA Hussen DF

Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2017 Jan 17; Vol. 5 (1), pp. 8-14. Date of Electronic Publication: 2017 Jan 17 (Print Publication: 2017).

Publication Type: Journal Article

Journal Info: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: eCollection Cited Medium: Print ISSN: 2324-9269 (Print) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: PubMed not MEDLINE