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Spinal muscular atrophy genetic epidemiology and the case for premarital genomic screening in Arab populations.
Commun Med (Lond). 2024 Jun 15;4(1):119. doi: 10.1038/s43856-024-00548-1.
Commun Med (Lond). 2024.
PMID: 38879606
Free PMC article.
The genomic landscape of rare disorders in the Middle East.
El Naofal M, Ramaswamy S, Alsarhan A, Nugud A, Sarfraz F, Janbaz H, Taylor A, Jain R, Halabi N, Yaslam S, Alfalasi R, Shenbagam S, Rabea F, Bitzan M, Yavuz L, Wafadari D, Abulhoul H, Shankar S, Al Maazmi M, Rizk R, Alloub Z, Elbashir H, Babiker MOE, Chencheri N, AlBanna A, Sultan M, El Bitar M, Kherani S, Thalange N, Alshryda S, Di Donato R, Tzivinikos C, Majid I, Freeman AF, Gonzalez C, Khan AO, Hamdan H, Abuhammour W, AlAwadhi M, AlKhayat A, Alsheikh-Ali A, Abou Tayoun AN.
El Naofal M, et al. Among authors: rabea f.
Genome Med. 2023 Jan 27;15(1):5. doi: 10.1186/s13073-023-01157-8.
Genome Med. 2023.
PMID: 36703223
Free PMC article.
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Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with Congenital Hypothyroidism: Ruling Out Recessive Inheritance or a Kinship/Laboratory Sequencing Error.
Jain R, Rabea F, Alfalasi R, Elabiary MW, Abou Tayoun A.
Jain R, et al. Among authors: rabea f.
J Appl Lab Med. 2023 Sep 7;8(5):993-999. doi: 10.1093/jalm/jfad039.
J Appl Lab Med. 2023.
PMID: 37478349
No abstract available.
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