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Genes & Development|December 1, 1989
Flexible recognition of rapidly evolving promoter sequences by mitochondrial transcription factor 1R P Fisher, M A Parisi, D A ClaytonThe Journal of Biological Chemistry|February 15, 1992
DNA wrapping and bending by a mitochondrial high mobility group-like transcriptional activator proteinR P Fisher, T Lisowsky, M A Parisi, et al.Nature|May 16, 1991
Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathiesJ F Hess, M A Parisi, J L Bennett, et al.Conservation Physiology|February 27, 2020
Can the impacts of cold-water pollution on fish be mitigated by thermal plasticity?M A Parisi, R L Cramp, M A Gordos, et al.American Journal of Human Genetics|December 5, 1998
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1A R Zinn, V S Tonk, Z Chen, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 17, 2003
Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangementsV L Souter, I A Glass, D B Chapman, et al.Journal of Medical Genetics|September 13, 2005
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.Journal of Medical Genetics|July 4, 2009
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)D Doherty, M A Parisi, L S Finn, et al.Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.Pageof 6