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Molecular Genetics & Genomic Medicine|September 5, 2019
The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communicationStephanie Harris, Allison L Cirino, Christina W Carr, et al.
Molecular Genetics & Genomic Medicine|August 20, 2019
Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in ChinaPeng Wang, Shirong Yu, Jianyong Liu, et al.
Molecular Genetics & Genomic Medicine|August 24, 2019
MiR-497-5p inhibits cell proliferation and metastasis in hepatocellular carcinoma by targeting insulin-like growth factor 1Guo-Shu Xu, Zi-Wei Li, Zhi-Ping Huang, et al.
Molecular Genetics & Genomic Medicine|September 27, 2019
Clinical and genetic analysis of ZTTK syndrome caused by SON heterozygous mutation c.394C>TYu Yang, Lei Xu, Zhen Yu, et al.
Molecular Genetics & Genomic Medicine|September 15, 2019
Metformin treatment in young children with fragile X syndromeHazel Maridith B Biag, Laura A Potter, Victoria Wilkins, et al.
Molecular Genetics & Genomic Medicine|February 28, 2019
Effects of MTNR1B genetic variants on the risk of type 2 diabetes mellitus: A meta-analysisLing-Long Shen, Yin Jin
Molecular Genetics & Genomic Medicine|November 6, 2018
Survival, causes of death, and cardiovascular events in patients with Marfan syndromeThy Thy Vanem, Odd Ragnar Geiran, Kirsten Krohg-Sørensen, et al.
Molecular Genetics & Genomic Medicine|November 6, 2018
Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contracturesMiriam Elbracht, Florian Kraft, Matthias Begemann, et al.
Molecular Genetics & Genomic Medicine|March 5, 2019
COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type IMingyuan Wang, Yi Guo, Pengfei Rong, et al.
Molecular Genetics & Genomic Medicine|February 21, 2019
Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case reportRamón Peces, Rocío Mena, Carlos Peces, et al.
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