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Clinical Genetics|December 17, 2016
Spectrum of ATP7B mutations and genotype-phenotype correlation in large-scale Chinese patients with Wilson DiseaseN Cheng, H Wang, W Wu, et al.Clinical Genetics|October 30, 2016
Maternal genetic polymorphisms and unexplained recurrent miscarriage: a systematic review and meta-analysisX Shi, X Xie, Y Jia, et al.Clinical Genetics|October 26, 2016
Genetic abnormalities leading to qualitative defects of sperm morphology or functionP F Ray, A Toure, C Metzler-Guillemain, et al.Clinical Genetics|October 26, 2016
The inheritance of juvenile onset primary open angle glaucomaV Gupta, B I Somarajan, S Gupta, et al.Clinical Genetics|October 26, 2016
Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1K Wimmer, T Rosenbaum, L MessiaenClinical Genetics|October 30, 2016
ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variantI Audo, S El Shamieh, C Méjécase, et al.Clinical Genetics|October 30, 2016
Emerging roles of RAC1 in treating lung cancer patientsT Zou, X Mao, J Yin, et al.Clinical Genetics|October 1, 1989
Batten disease (Spielmeyer-Sjøgren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16H Eiberg, R M Gardiner, J MohrClinical Genetics|December 20, 2016
Myotonic dystrophy type 1: role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and molecular diagnosisM Santoro, M Masciullo, G Silvestri, et al.Pageof 719