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BMC Medical Genomics|June 15, 2019
Prenatal identification of partial 3q duplication syndromeMagdalena Pasińska, Rafał Adamczak, Anna Repczyńska, et al.BMC Medical Genomics|October 31, 2021
CTNNA3 genetic polymorphism may be a new genetic signal of type 2 diabetes in the Chinese Han population: a case control studyYunjun Zhang, Xiaoman Zhou, Wanjuan Dai, et al.BMC Medical Genomics|October 31, 2021
Analysis of multiple gene co-expression networks to discover interactions favoring CFTR biogenesis and ΔF508-CFTR rescueMatthew D Strub, Long Gao, Kai Tan, et al.BMC Medical Genomics|June 28, 2019
Development and validation of GMI signature based random survival forest prognosis model to predict clinical outcome in acute myeloid leukemiaMingguang Shi, Guofu XuBMC Medical Genomics|July 11, 2019
Retroposed copies of RET gene: a somatically acquired event in medullary thyroid carcinomaLarissa V Bim, Fábio C P Navarro, Flávia O F Valente, et al.BMC Medical Genomics|October 26, 2021
PDX1 and MC4R genetic polymorphisms are associated with type 2 diabetes mellitus risk in the Chinese Han populationNing Wang, Rui Tong, Jing Xu, et al.BMC Medical Genomics|March 5, 2022
Li-Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype-phenotype correlationHela Sassi, Rym Meddeb, Mohamed Aziz Cherif, et al.BMC Medical Genomics|March 5, 2022
Acceleration of the DNA methylation clock among lynch syndrome-associated mutation carriersMarta Cuadros, Carlos Cano, Sonia Garcia-Rodriguez, et al.BMC Medical Genomics|March 7, 2022
In silico drug repositioning based on integrated drug targets and canonical correlation analysisHailin Chen, Zuping Zhang, Jingpu ZhangBMC Medical Genomics|March 4, 2022
Attenuated clinical and osteoclastic phenotypes of Paget's disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 geneMariam Dessay, Emile Couture, Halim Maaroufi, et al.Pageof 276