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Genomics|August 1, 1989
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17A G Menon, D H Ledbetter, D C Rich, et al.American Journal of Human Genetics|January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17J W Fountain, M R Wallace, A M Brereton, et al.Science (New York, N.Y.)|July 26, 1996
Multicolor spectral karyotyping of human chromosomesE Schröck, S du Manoir, T Veldman, et al.Genomics|September 11, 1991
Assignment of the human prohibitin gene (PHB) to chromosome 17 and identification of a DNA polymorphismJ J White, D H Ledbetter, R L Eddy, et al.Prenatal Diagnosis|May 1, 1992
Chorionic mosaicism: association with fetal loss but not with adverse perinatal outcomeR J Wapner, J L Simpson, M S Golbus, et al.American Journal of Ophthalmology|November 15, 1991
A sibship with unusual anomalies of the eye and skeleton (Michels' syndrome)M A De La Paz, R A Lewis, J R Patrinely, et al.Cell Death & Disease|January 1, 2016
Synergistic killing of human small cell lung cancer cells by the Bcl-2-inositol 1,4,5-trisphosphate receptor disruptor BIRD-2 and the BH3-mimetic ABT-263E F Greenberg, K S McColl, F Zhong, et al.Iscience|May 25, 2026
Extracellular vesicle transcriptomic analysis to investigate muscle adaptation in microgravitySamantha Ali, Maddalena Parafati, Zachary F Greenberg, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Urinary extracellular vesicles for high-precision bladder cancer subtyping and prognosisZachary F Greenberg, Tarun E Hutchinson, Johnathan Kahn, et al.Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.Pageof 33