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BMC Medical Genomics|August 2, 2020
A novel use for Levey-Jennings charts in prenatal molecular diagnosisBinghuan Weng, Ya-Li Xu, Jun Ying, et al.
BMC Medical Genomics|April 22, 2021
Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case reportYoussef El Kadiri, Ilham Ratbi, Fatima Zahra Laarabi, et al.
BMC Medical Genomics|April 14, 2021
Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disordersYan Sun, Fengxia Liu, Chunna Fan, et al.
BMC Medical Genomics|April 15, 2021
Comprehensive tumor molecular profile analysis in clinical practiceMustafa Özdoğan, Eirini Papadopoulou, Nikolaos Tsoulos, et al.
BMC Medical Genomics|April 10, 2021
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomaliesXuejiao Chen, Huihui Xu, Weiwu Shi, et al.
BMC Medical Genomics|March 28, 2013
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patientsBente A Talseth-Palmer, Elizabeth G Holliday, Tiffany-Jane Evans, et al.
BMC Medical Genomics|May 15, 2012
A target based approach identifies genomic predictors of breast cancer patient response to chemotherapyRobin M Hallett, Gregory Pond, John A Hassell
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