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Human Genetics|January 1, 1995
Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneityE C Mariman, S E van Beersum, C W Cremers, et al.Journal of Lipid Research|September 1, 1988
Identification of apolipoprotein E polymorphism by using synthetic oligonucleotidesH J Smeets, J Poddighe, P M Stuyt, et al.Nephron|January 1, 1988
Linkage of X-linked nephrogenic diabetes insipidus with DXS52, a polymorphic DNA markerN Knoers, H vd Heyden, B A von Oost, et al.Human Genetics|January 1, 1985
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosomeL M Bleeker-Wagemakers, U Friedrich, A Gal, et al.Human Genetics|January 1, 1983
Cloning of genomic sequences from the human Y chromosome after purification by dual beam flow sortingC R Müller, K E Davies, C Cremer, et al.Human Molecular Genetics|February 1, 1994
Localization of the gene for dominant cystoid macular dystrophy on chromosome 7pH Kremer, A Pinckers, B van den Helm, et al.Nature|October 18, 1990
Cloning of a gene that is rearranged in patients with choroideraemiaF P Cremers, D J van de Pol, L P van Kerkhoff, et al.American Journal of Medical Genetics|July 15, 1994
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studiesB C Hamel, E C Mariman, S E van Beersum, et al.FEBS Letters|November 7, 1988
Assignment of the human aminopeptidase N (peptidase E) gene to chromosome 15q13-qterT A Kruse, L Bolund, K H Grzeschik, et al.Cytogenetics and Cell Genetics|January 1, 1988
Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19T Hulsebos, D Schonk, I van Dalen, et al.Pageof 21