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Chromosoma|November 1, 1995
Human gamma X satellite DNA: an X chromosome specific centromeric DNA sequenceC Lee, X Li, E W Jabs, et al.Chromosoma|May 1, 1991
Studies of mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanismE W Jabs, C M Tuck-Muller, R Cusano, et al.The Journal of Biological Chemistry|April 15, 1991
Characterization of an alpha 1----3-galactosyltransferase homologue on human chromosome 12 that is organized as a processed pseudogeneD H Joziasse, J H Shaper, E W Jabs, et al.Genomics|December 10, 1999
Genomic organization, expression, and chromosome location of the human SNAIL gene (SNAI1) and a related processed pseudogene (SNAI1P)W A Paznekas, K Okajima, M Schertzer, et al.American Journal of Medical Genetics|December 18, 2001
Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 geneR B Lowry, E W Jabs, G E Graham, et al.Journal of Neurochemistry|December 1, 1994
Partial structure and mapping of the human myelin P2 protein geneV Narayanan, B Ripepi, E W Jabs, et al.The Journal of Biological Chemistry|July 25, 1993
The human aquaporin-CHIP gene. Structure, organization, and chromosomal localizationC Moon, G M Preston, C A Griffin, et al.Prenatal Diagnosis|February 1, 1992
Prenatal identification of small mosaic markers of different chromosomal originsG Stetten, K J Blakemore, A M Courter, et al.American Journal of Medical Genetics|April 1, 1992
Partial gonadal dysgenesis in a patient with a marker Y chromosomeP Y Fechner, K D Smith, E W Jabs, et al.Nature Genetics|December 1, 1995
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricansG A Meyers, S J Orlow, I R Munro, et al.Pageof 11