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Turner syndrome in diverse populations.
Am J Med Genet A. 2020 Feb;182(2):303-313. doi: 10.1002/ajmg.a.61461. Epub 2019 Dec 19.
Am J Med Genet A. 2020.
PMID: 31854143
Free PMC article.
Williams-Beuren syndrome in diverse populations.
Kruszka P, Porras AR, de Souza DH, Moresco A, Huckstadt V, Gill AD, Boyle AP, Hu T, Addissie YA, Mok GTK, Tekendo-Ngongang C, Fieggen K, Prijoles EJ, Tanpaiboon P, Honey E, Luk HM, Lo IFM, Thong MK, Muthukumarasamy P, Jones KL, Belhassan K, Ouldim K, El Bouchikhi I, Bouguenouch L, Shukla A, Girisha KM, Sirisena ND, Dissanayake VHW, Paththinige CS, Mishra R, Kisling MS, Ferreira CR, de Herreros MB, Lee NC, Jamuar SS, Lai A, Tan ES, Ying Lim J, Wen-Min CB, Gupta N, Lotz-Esquivel S, Badilla-Porras R, Hussen DF, El Ruby MO, Ashaat EA, Patil SJ, Dowsett L, Eaton A, Innes AM, Shotelersuk V, Badoe Ë, Wonkam A, Obregon MG, Chung BHY, Trubnykova M, La Serna J, Gallardo Jugo BE, Chávez Pastor M, Abarca Barriga HH, Megarbane A, Kozel BA, van Haelst MM, Stevenson RE, Summar M, Adeyemo AA, Morris CA, Moretti-Ferreira D, Linguraru MG, Muenke M.
Kruszka P, et al. Among authors: hussen df.
Am J Med Genet A. 2018 May;176(5):1128-1136. doi: 10.1002/ajmg.a.38672.
Am J Med Genet A. 2018.
PMID: 29681090
Free PMC article.
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Rubinstein-Taybi syndrome in diverse populations.
Tekendo-Ngongang C, Owosela B, Fleischer N, Addissie YA, Malonga B, Badoe E, Gupta N, Moresco A, Huckstadt V, Ashaat EA, Hussen DF, Luk HM, Lo IFM, Hon-Yin Chung B, Fung JLF, Moretti-Ferreira D, Batista LC, Lotz-Esquivel S, Saborio-Rocafort M, Badilla-Porras R, Penon Portmann M, Jones KL, Abdul-Rahman OA, Uwineza A, Prijoles EJ, Ifeorah IK, Llamos Paneque A, Sirisena ND, Dowsett L, Lee S, Cappuccio G, Kitchin CS, Diaz-Kuan A, Thong MK, Obregon MG, Mutesa L, Dissanayake VHW, El Ruby MO, Brunetti-Pierri N, Ekure EN, Stevenson RE, Muenke M, Kruszka P.
Tekendo-Ngongang C, et al. Among authors: hussen df.
Am J Med Genet A. 2020 Dec;182(12):2939-2950. doi: 10.1002/ajmg.a.61888. Epub 2020 Sep 27.
Am J Med Genet A. 2020.
PMID: 32985117
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Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
Hussen DF, Kamel AK, Mekkawy MK, Ashaat EA, El Ruby MO.
Hussen DF, et al.
Mol Syndromol. 2020 Dec;11(5-6):284-295. doi: 10.1159/000510428. Epub 2020 Sep 23.
Mol Syndromol. 2020.
PMID: 33510599
Free PMC article.
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Genetics and Genomic Medicine in Egypt: steady pace.
Temtamy SA, Hussen DF.
Temtamy SA, et al. Among authors: hussen df.
Mol Genet Genomic Med. 2017 Jan 17;5(1):8-14. doi: 10.1002/mgg3.271. eCollection 2017 Jan.
Mol Genet Genomic Med. 2017.
PMID: 28116325
Free PMC article.
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The Micronuclei Scoring as a Biomarker for Early Detection of Genotoxic Effect of Cigarette Smoking.
Mohammed AM, Hussen DF, Rashad H, Hasheesh A.
Mohammed AM, et al. Among authors: hussen df.
Asian Pac J Cancer Prev. 2020 Jan 1;21(1):87-92. doi: 10.31557/APJCP.2020.21.1.87.
Asian Pac J Cancer Prev. 2020.
PMID: 31983169
Free PMC article.
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The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy.
Ashaat EA, Ahmed HA, Elaraby NM, Fayez A, Metwally AM, Mekkawy MK, Hussen DF, Ashaat NA, Elhossini RM, ElAwady HA, Abdelgawad RHA, Gammal ME, Al Kersh MA, Saleh DA.
Ashaat EA, et al. Among authors: hussen df.
Mol Neurobiol. 2023 Dec 28. doi: 10.1007/s12035-023-03866-y. Online ahead of print.
Mol Neurobiol. 2023.
PMID: 38153683
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