Faten Moassass
United States Atomic Energy Commission
39 Papers
98 Citations
Faten Moassass is an academic researcher from United States Atomic Energy Commission. The author has contributed to research in topics: Myeloid leukemia & Chromosomal translocation. The author has an hindex of 8, co-authored 35 publications. Previous affiliations of Faten Moassass include University of Jena.
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Papers
Influence of CYP1A1, GST polymorphisms and susceptibility risk of chronic myeloid leukemia in Syrian population.
TL;DR: Logistic regression analyses showed significant risk of CML associated with CYP1A1 Val allele, suggesting that the association of the GSTM1 null genotype, either alone or in combination with GSTT1 null, with CyP1AI heterozygous leads to the CML risk.
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Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males
TL;DR: The higher frequency of AZF deletions in this study was comparable with frequencies in other countries and regions of the world, possibly due to the elevated number of the sequence-tagged site (STS) markers used for this screening.
Mutations of the Connexin 26 gene in families with non-syndromic hearing loss.
TL;DR: The data revealed a high prevalence of the 35delG mutation among deaf families and important implications for the diagnosis and counseling of families with Cx26 deafness.
•Journal Article
Correlation of p210 BCR-ABL transcript variants with clinical, parameters and disease outcome in 45 chronic myeloid leukemia patients.
TL;DR: The distribution BCR-ABL1 transcript types found in Syria were similar to that of Indian Far-Eastern, African or European populations and the M-BCR rearrangement types were not dependent on white blood count, platelet count, hemoglobin level or gender of the patients.
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Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl
TL;DR: Attempts for genotype-phenotype correlations for partial trisomy 9p might have been hampered by the fact that more complex, cryptic aberrations were neither considered nor detected in comparable clinical cases.