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M Tuck

Showing results (111-120 of 159) with videos related to

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Human Genetics|May 1, 1993
Duplication of the short arm of the X chromosome in mother and daughterC M Tuck-Muller, J E Martinez, D A Batista, et al.
British Journal of Obstetrics and Gynaecology|February 1, 1987
Prophylactic blood transfusion in maternal sickle cell syndromesS M Tuck, C E James, E M Brewster, et al.
The International Journal of Biochemistry|January 1, 1989
Site-specificity of histone H1 methylation by two H1-specific protein-lysine N-methyltransferases from Euglena gracilisB F Frost, K S Park, M Tuck, et al.
Circulation Research|June 1, 1975
A circulating renin activator in essential hypertensionM P Sambhi, P Eggena, J C Barrett, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22W Ahmad, S Li, H Chen, et al.
American Journal of Medical Genetics|January 25, 2002
Molecular characterization of a ring chromosome 16 from a patient with bilateral cataractsWeigong He, Cathy M Tuck-Muller, José E Martínez, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1983
Plasma corticosteroids in hyperreninemic hypoaldosteronism: evidence for diffuse impairment of the zona glomerulosaN Stern, F W Beck, J R Sowers, et al.
American Journal of Medical Genetics|January 8, 1999
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)S Li, C M Tuck-Muller, J E Martínez, et al.
AJR. American Journal of Roentgenology|April 1, 1984
Prenatal observation of umbilical cord hematomaW H Sutro, S M Tuck, A Loesevitz, et al.
Chromosoma|April 28, 2005
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cellsDavid Gisselsson, Chunbo Shao, Cathy M Tuck-Muller, et al.
Pageof 16

Showing results (111-120 of 159) with videos related to

Sort By:
Pageof 16
Human Genetics|May 1, 1993
Duplication of the short arm of the X chromosome in mother and daughterC M Tuck-Muller, J E Martinez, D A Batista, et al.
British Journal of Obstetrics and Gynaecology|February 1, 1987
Prophylactic blood transfusion in maternal sickle cell syndromesS M Tuck, C E James, E M Brewster, et al.
The International Journal of Biochemistry|January 1, 1989
Site-specificity of histone H1 methylation by two H1-specific protein-lysine N-methyltransferases from Euglena gracilisB F Frost, K S Park, M Tuck, et al.
Circulation Research|June 1, 1975
A circulating renin activator in essential hypertensionM P Sambhi, P Eggena, J C Barrett, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22W Ahmad, S Li, H Chen, et al.
American Journal of Medical Genetics|January 25, 2002
Molecular characterization of a ring chromosome 16 from a patient with bilateral cataractsWeigong He, Cathy M Tuck-Muller, José E Martínez, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1983
Plasma corticosteroids in hyperreninemic hypoaldosteronism: evidence for diffuse impairment of the zona glomerulosaN Stern, F W Beck, J R Sowers, et al.
American Journal of Medical Genetics|January 8, 1999
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)S Li, C M Tuck-Muller, J E Martínez, et al.
AJR. American Journal of Roentgenology|April 1, 1984
Prenatal observation of umbilical cord hematomaW H Sutro, S M Tuck, A Loesevitz, et al.
Chromosoma|April 28, 2005
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cellsDavid Gisselsson, Chunbo Shao, Cathy M Tuck-Muller, et al.
Pageof 16