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Molecular Genetics & Genomic Medicine|December 12, 2022
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature reviewJianlong Zhuang, Qi Luo, Meihua Xie, et al.
Molecular Genetics & Genomic Medicine|September 22, 2020
Identification of common differentially expressed genes in Turner (45,X) and Klinefelter (47,XXY) syndromes using bioinformatics analysisMaría Carolina Manotas, Juan Camilo Calderón, Liliana López-Kleine, et al.
Molecular Genetics & Genomic Medicine|April 8, 2020
Genetic and molecular biology of bladder cancer among Iranian patientsMajid Mojarrad, Meysam Moghbeli
Molecular Genetics & Genomic Medicine|September 12, 2020
Haploinsufficiency as a disease mechanism in GNB1-associated neurodevelopmental disorderLaura Schultz-Rogers, Ikuo Masuho, Filippo Pinto E Vairo, et al.
Molecular Genetics & Genomic Medicine|December 23, 2019
An innovative panel containing a set of insertion/deletion loci for individual identification and its forensic efficiency evaluations in Chinese Hui ethnic minorityWei Cui, Xiaoye Jin, Yuxin Guo, et al.
Molecular Genetics & Genomic Medicine|December 24, 2019
The role of race and ethnicity in views toward and participation in genetic studies and precision medicine research in the United States: A systematic review of qualitative and quantitative studiesElena R Fisher, Rebekah Pratt, Riley Esch, et al.
Molecular Genetics & Genomic Medicine|March 30, 2020
Sleep patterns and problems among children with 22q11 deletion syndromeJill M Arganbright, Meghan Tracy, Susan Starling Hughes, et al.
Molecular Genetics & Genomic Medicine|March 11, 2020
Molecular characterization of hemophilia B patients in ColombiaYolima A Parrado Jara, Luz K Yunis Hazbun, Adriana Linares, et al.
Molecular Genetics & Genomic Medicine|January 25, 2020
Aromatic L-amino acid decarboxylase deficiency in 17 Mainland China patients: Clinical phenotype, molecular spectrum, and therapy overviewWeiqian Dai, Deyun Lu, Xuefan Gu, et al.
Molecular Genetics & Genomic Medicine|October 8, 2020
Whole-exome sequencing identified two novel mutations of DYNC2LI1 in fetal skeletal ciliopathyXinyue Zhang, Yanqin You, Xiaoxiao Xie, et al.
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