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CJC Open|December 30, 2024
Transfabric Leaks After Percutaneous Left Atrial Appendage Occlusion Procedures with the WATCHMAN FLX DeviceNicholas J C Bauer, Abdullah F Alfawaz, Lan-Chau Kha, et al.Genomics|April 1, 1992
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28G G Consalez, C L Stayton, N B Freimer, et al.Acta Ophthalmologica|April 8, 2022
Clinical outcomes of treatment with idebenone in Leber's hereditary optic neuropathy in the Netherlands: A national cohort studyJudith A M van Everdingen, Jan Willem R Pott, Noël J C Bauer, et al.Clinical Genetics|October 27, 1998
Two common mutations in the CLN2 gene underlie late infantile neuronal ceroid lipofuscinosisN Zhong, K E Wisniewski, J Hartikainen, et al.American Journal of Medical Genetics|April 20, 1999
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detectionC Dobkin, X Ding, S Li, et al.Genetic Testing|January 6, 2001
Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinosesN A Zhong, K E Wisniewski, W Ju, et al.Genes, Brain, and Behavior|May 21, 2011
Association of upregulated Ras/Raf/ERK1/2 signaling with autismH Zou, Y Yu, A M Sheikh, et al.Indian Journal of Ophthalmology|November 24, 2020
Phakic intraocular lenses: An overviewSoraya M R Jonker, Tos T J M Berendschot, Isabelle E Y Saelens, et al.Nature Genetics|July 1, 1992
Evidence of founder chromosomes in fragile X syndromeR I Richards, K Holman, K Friend, et al.American Journal of Medical Genetics|January 1, 1986
High dose folic acid treatment of fragile (X) malesW T Brown, I L Cohen, G S Fisch, et al.Pageof 23