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Molecular Genetics & Genomic Medicine|May 29, 2021
Polymorphisms in the CYP2A6 and ABCC4 genes are associated with a protective effect on chronic myeloid leukemia in the Brazilian Amazon populationNatasha Monte, Karla B C C Pantoja, Juliana C G Rodrigues, et al.
Molecular Genetics & Genomic Medicine|June 9, 2021
Genetic variations in DNA repair gene NEIL1 associated with radiation pneumonitis risk in lung cancer patientsYuming Zheng, Leizhen Zheng, Jiahua Yu, et al.
Molecular Genetics & Genomic Medicine|May 27, 2021
Genetic polymorphism of vitamin D receptors and plasminogen activator inhibitor-1 and osteonecrosis risk in childhood acute lymphoblastic leukemiaLaila M Sherief, Mohamed Beshir, Nermin Raafat, et al.
Molecular Genetics & Genomic Medicine|October 5, 2020
Atypical juvenile hereditary hemochromatosis onset with positive pancreatic islet autoantibodies diabetes caused by novel mutations in HAMP and overall clinical managementHui-Xuan Wu, Jun-Ying Liu, De-Wen Yan, et al.
Molecular Genetics & Genomic Medicine|January 4, 2020
Two novel mutations of COL1A1 in fetal genetic skeletal dysplasia of ChineseRuibing Li, Jianan Wang, Longxia Wang, et al.
Molecular Genetics & Genomic Medicine|December 20, 2022
Prevalence and clinical implications of germline mutations among Jordanian patients with ovarian cancer. The Jordanian exploratory cancer genetics (Jo-ECAG) ovarian studyHikmat Abdel-Razeq, Khansa Al-Azzam, Shatha Elemian, et al.
Molecular Genetics & Genomic Medicine|June 14, 2022
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian familyAbdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, et al.
Molecular Genetics & Genomic Medicine|June 3, 2022
Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndromeLilia Kraoua, Hager Jaouadi, Mohamed Allouche, et al.
Molecular Genetics & Genomic Medicine|June 6, 2022
Next-generation sequencing in identification of pathogenic variants in primary hyperoxaluria among 21 Egyptian families: Identification of two novel AGXT gene mutationsHoda A Ahmed, Fatina I Fadel, Mohamed A Abdel Mawla, et al.
Molecular Genetics & Genomic Medicine|December 3, 2022
Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462Lauren Brady, Mark Ballantyne, John Duck, et al.
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