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Molecular Genetics & Genomic Medicine|May 14, 2020
Human closed and open apex premolar teeth express different toll-like receptorReza Jafari, Razieh Karamzadeh, Faezeh Pesaran Hajabbas, et al.
Molecular Genetics & Genomic Medicine|May 19, 2020
The pedigree analysis and prenatal diagnosis of Hong Kongαα Thalassemia and the sequence analysis of Hong Kongαα AlleleWenjuan Wang, Haiqing Zheng, Dan Zeng, et al.
Molecular Genetics & Genomic Medicine|May 9, 2020
A novel variant of the IFITM5 gene within the 5'-UTR causes neonatal transverse clavicular fracture: Expanding the genetic spectrumDong Wu, Yuxin Wang, Huijuan Huang
Molecular Genetics & Genomic Medicine|May 9, 2020
Shortened consent forms for genome-wide sequencing: Parent and provider perspectivesEmma C Hitchcock, Causes Study, Alison M Elliott
Molecular Genetics & Genomic Medicine|August 18, 2021
Case report of the first molecular diagnosis of Stickler syndrome with a pathogenic COL2A1 variant in a Mongolia familyHong Wu, Songtian Che, Shuchun Li, et al.
Molecular Genetics & Genomic Medicine|August 23, 2021
Identification of a novel COL10A1: c.1952 G>T variant in a family with Schmid metaphyseal chondrodysplasia and development of a noninvasive prenatal testing methodYanchou Ye, Weihao Li, Guan Wang, et al.
Molecular Genetics & Genomic Medicine|June 24, 2020
Disrupted minor intron splicing is prevalent in Mendelian disordersAnouk M Olthof, Jeffrey S Rasmussen, Philippe M Campeau, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese populationWen Huang, Qiuping Xia, Shiyu Luo, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer riskConor Smyth, Iva Špakulová, Owen Cotton-Barratt, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Contiguous mutation syndrome in the era of high-throughput sequencingMaéva Langouët, Karine Siquier-Pernet, Sylvia Sanquer, et al.
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