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Annals of Human Genetics|December 4, 2003
A 34 bp deletion within TSC2 is a rare polymorphism, not a pathogenic mutationPenelope S Roberts, Vijaya Ramesh, Sandra Dabora, et al.American Journal of Perinatology|August 1, 2019
High Fetal Fraction on First Trimester Cell-Free DNA Aneuploidy Screening and Adverse Pregnancy OutcomesLydia L Shook, Mark A Clapp, Penelope S Roberts, et al.American Journal of Perinatology|November 19, 2019
Low Fetal Fraction and Birth Weight in Women with Negative First-Trimester Cell-Free DNA ScreeningMark A Clapp, Margaret Berry, Lydia L Shook, et al.Human Genetics|July 24, 2002
SNP identification, haplotype analysis, and parental origin of mutations in TSC2Penelope S Roberts, Joon Chung, Sergiusz Jozwiak, et al.Journal of Neuropathology and Experimental Neurology|December 31, 2004
Pathogenesis of tuberous sclerosis subependymal giant cell astrocytomas: biallelic inactivation of TSC1 or TSC2 leads to mTOR activationJennifer A Chan, Hongbing Zhang, Penelope S Roberts, et al.Pageof 1