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Molecular Genetics & Genomic Medicine|April 23, 2019
Myeloid malignancies-related somatic mutations in aging individualsDiego F Coutinho, Ilana R Zalcberg, Bárbara C R Monte-Mór
Molecular Genetics & Genomic Medicine|February 25, 2022
A nonsense mutation in MME gene associates with autosomal recessive late-onset Charcot-Marie-Tooth diseaseZeinab Jamiri, Rana Khosravi, Mohammad Mehdi Heidari, et al.
Molecular Genetics & Genomic Medicine|February 14, 2022
Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patientsJianbo Zhao, Guizhen Lyu, Changhong Ding, et al.
Molecular Genetics & Genomic Medicine|May 7, 2019
PMS2 germline mutation c.943C>T (p.Arg315*)-induced Lynch syndrome-associated ovarian cancerXiaoqing Guo, Weimin Wu, Hao Gao, et al.
Molecular Genetics & Genomic Medicine|January 3, 2023
Involvement of ERCC1 (rs3212986) and ERCC2 (rs1799793, rs13181) polymorphisms of DNA repair genes in breast cancer occurrence in Burkina FasoMarc Donald Wilfried Adico, Abdou Azaque Zouré, Herman Karim Sombié, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
Forensic features and genetic background exploration of a new 47-autosomal InDel panel in five representative Han populations residing in Northern ChinaFeng Song, Min Lang, Luyao Li, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
Complicated ventricular arrhythmia and hematologic myeloproliferative disorder in RIT1-associated Noonan syndrome: Expanding the phenotype and review of the literatureSafwat A Aly, Kenneth M Boyer, Brie-Ann A Muller, et al.
Molecular Genetics & Genomic Medicine|May 15, 2020
Acromicric dysplasia with stiff skin syndrome-like severe cutaneous presentation in an 8-year-old boy with a missense FBN1 mutation: Case report and literature reviewTao Wang, Yuyan Yang, Qi Dong, et al.
Molecular Genetics & Genomic Medicine|May 14, 2020
Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature reviewYaobin Liu, Beth Mapow
Molecular Genetics & Genomic Medicine|May 14, 2020
Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld-Rieger syndromeValeria Lo Faro, Sorath N Siddiqui, Muhammad I Khan, et al.
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