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Molecular Genetics & Genomic Medicine|January 23, 2020
SCD rs41290540 single-nucleotide polymorphism modifies miR-498 binding and is associated with a decreased risk of coronary artery diseaseZhou Liu, Xiaojian Yin, Hui Mai, et al.
Molecular Genetics & Genomic Medicine|March 12, 2018
Dyssegmental dysplasia, Silverman-Handmaker type: A challenging antenatal diagnosis in a dizygotic twin pregnancyShuaa Basalom, Yannis Trakadis, Roberta Shear, et al.
Molecular Genetics & Genomic Medicine|February 15, 2019
Molecular diagnosis of somatic overgrowth conditions: A single-center experienceEmilie Lalonde, Jessica Ebrahimzadeh, Keith Rafferty, et al.
Molecular Genetics & Genomic Medicine|November 27, 2018
Gene coexpression network analysis identified potential biomarkers in gestational diabetes mellitus progressionXiaomin Zhao, Wen Li
Molecular Genetics & Genomic Medicine|March 25, 2018
A rapid and reliable chromosome analysis method for products of conception using interphase nucleiRamesh Babu, Daniel L Van Dyke, Saurabh Bhattacharya, et al.
Molecular Genetics & Genomic Medicine|January 26, 2019
Interaction of germline variants in a family with a history of early-onset clear cell renal cell carcinomaEmmanuelle Nicolas, Elena V Demidova, Waleed Iqbal, et al.
Molecular Genetics & Genomic Medicine|February 8, 2018
Association between glutathione peroxidase 1 codon 198 variant and the occurrence of breast cancer in RwandaThierry Habyarimana, Youssef Bakri, Pacifique Mugenzi, et al.
Molecular Genetics & Genomic Medicine|January 25, 2018
Functional study of a novel missense single-nucleotide variant of NUP107 in two daughters of Mexican origin with premature ovarian insufficiencyYu Ren, Feiyang Diao, Sunita Katari, et al.
Molecular Genetics & Genomic Medicine|January 26, 2018
Experience with genomic sequencing in pediatric patients with congenital cardiac defects in a large community hospitalNatalie S Hauser, Benjamin D Solomon, Thierry Vilboux, et al.
Molecular Genetics & Genomic Medicine|January 30, 2018
Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiencyXiao-Wen Yang, Wen-Bin He, Fei Gong, et al.
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