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Molecular Genetics & Genomic Medicine|May 26, 2018
Next-generation sequencing unravels extensive genetic alteration in recurrent ovarian cancer and unique genetic changes in drug-resistant recurrent ovarian cancerZhen-Hua Du, Fang-Fang Bi, Lei Wang, et al.
Molecular Genetics & Genomic Medicine|May 29, 2018
Genetics in mainstream medicine: Finally within grasp to influence healthcare globallySwaroop Aradhya, Robert L Nussbaum
Molecular Genetics & Genomic Medicine|May 18, 2018
Whole-exome sequencing for variant discovery in blepharospasmJun Tian, Satya R Vemula, Jianfeng Xiao, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri LankaShari Javadiyan, Sionne E M Lucas, Dechen Wangmo, et al.
Molecular Genetics & Genomic Medicine|May 21, 2018
Co-occurrence of schwannomatosis and rhabdoid tumor predisposition syndrome 1Hildegard Kehrer-Sawatzki, Uwe Kordes, Simone Seiffert, et al.
Molecular Genetics & Genomic Medicine|May 3, 2018
Heart failure and sudden cardiac death in heritable thoracic aortic disease caused by pathogenic variants in the SMAD3 geneJulie De Backer, Alan C Braverman
Molecular Genetics & Genomic Medicine|July 27, 2018
Using exome sequencing to decipher family history in a healthy individual: Comparison of pathogenic and population MTM1 variantsMonica Penon, Hengameh Zahed, Victoria Berger, et al.
Molecular Genetics & Genomic Medicine|July 12, 2018
Nearly complete genome sequence of one GII.17 Norovirus identified by direct sequencing from HuZhou, ChinaLei Ji, Liping Chen, Deshun Xu, et al.
Molecular Genetics & Genomic Medicine|July 5, 2018
Signs indicating dementia in Down, Williams and Fragile X syndromesOili Sauna-Aho, Nina Bjelogrlic-Laakso, Auli Siren, et al.
Molecular Genetics & Genomic Medicine|July 23, 2018
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known geneGigliola Di Matteo, Maria Chiriaco, Alessia Scarselli, et al.
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