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Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients.
Nawaz H, Parveen A, Khan SA, Zalan AK, Khan MA, Muhammad N, Hassib NF, Mostafa MI, Elhossini RM, Roshdy NN, Ullah A, Arif A, Khan S, Ammerpohl O, Wasif N. Nawaz H, et al. Among authors: elhossini rm. Heliyon. 2023 Dec 14;10(1):e23688. doi: 10.1016/j.heliyon.2023.e23688. eCollection 2024 Jan 15. Heliyon. 2023. PMID: 38192829 Free PMC article.
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: elhossini rm. Mol Neurobiol. 2023 Dec 28. doi: 10.1007/s12035-023-03866-y. Online ahead of print. Mol Neurobiol. 2023. PMID: 38153683