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Molecular Genetics & Genomic Medicine|September 20, 2018
Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in ChinaDan Zhao, Ailu Cai, Bing Wang, et al.Molecular Genetics & Genomic Medicine|September 29, 2018
Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9Sara C M Stoof, Rogier Kersseboom, Femke A T de Vries, et al.Molecular Genetics & Genomic Medicine|April 11, 2019
Clinical utility in infants with suspected monogenic conditions through next-generation sequencingSha Hong, Li Wang, Dongying Zhao, et al.Molecular Genetics & Genomic Medicine|April 11, 2019
HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusionMaolian Gong, Yong Yu, Lei Liang, et al.Molecular Genetics & Genomic Medicine|April 11, 2019
Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high-risk breast cancerXiaozhen Wang, Haimeng Liu, Amina Maimaitiaili, et al.Molecular Genetics & Genomic Medicine|April 12, 2019
CCDN1 rs603965 polymorphism may serve as a genetic biomarker of brain tumor: A meta-analysis of 5,769 subjectsJiarong Lan, Min Li, Haifeng WangMolecular Genetics & Genomic Medicine|August 13, 2018
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patientsThomas Eggermann, Susanne Ledig, Matthias Begemann, et al.Molecular Genetics & Genomic Medicine|April 7, 2018
Fragile X checklists: A meta-analysis and development of a simplified universal clinical checklistToni Kasole Lubala, Aimé Lumaka, Gray Kanteng, et al.Molecular Genetics & Genomic Medicine|May 28, 2019
Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjectsZhaowei Zhou, Ke Wang, Juan Zhou, et al.Molecular Genetics & Genomic Medicine|May 16, 2019
Autosomal dominant mitochondrial membrane protein-associated neurodegeneration (MPAN)Allison Gregory, Mitesh Lotia, Suh Young Jeong, et al.Pageof 252