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C M Tuck-Muller

Showing results (11-20 of 33) with videos related to

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American Journal of Medical Genetics|February 6, 1999
1p microdeletion in sibs with minimal phenotypic manifestationsJ E Martínez, C M Tuck-Muller, W Gasparrini, et al.
Stain Technology|September 1, 1984
A method for combined C-banding and silver stainingC M Tuck-Muller, B L Bordson, M M Kane, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Correction of sphingomyelinase deficiency in Niemann-Pick type C fibroblasts by removal of lipoprotein fraction from culture mediaG H Thomas, C M Tuck-Muller, C S Miller, et al.
Leukemia|January 1, 1992
Cancer susceptibility in ataxia-telangiectasiaR D Peterson, J D Funkhouser, C M Tuck-Muller, et al.
Journal of Medical Genetics|January 5, 2002
High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sampleM Ehrlich, F Tsien, D Herrera, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Chromosome studies in 10 patients with the Rett syndromeJ W Moore, C M Tuck-Muller, M Murphy, et al.
American Journal of Medical Genetics|May 17, 1996
A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspringC M Tuck-Muller, M Varela, S Li, et al.
American Journal of Medical Genetics|March 9, 1999
Adrenal insufficiency in Smith-Lemli-Opitz syndromeH C Andersson, J Frentz, J E Martínez, et al.
American Journal of Medical Genetics|June 5, 1995
Translocation 10;18 in a patient with juvenile neuronal ceroid-lipofuscinosis (Batten disease)C M Tuck-Muller, P R Dyken, S Li, et al.
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.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|February 6, 1999
1p microdeletion in sibs with minimal phenotypic manifestationsJ E Martínez, C M Tuck-Muller, W Gasparrini, et al.
Stain Technology|September 1, 1984
A method for combined C-banding and silver stainingC M Tuck-Muller, B L Bordson, M M Kane, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Correction of sphingomyelinase deficiency in Niemann-Pick type C fibroblasts by removal of lipoprotein fraction from culture mediaG H Thomas, C M Tuck-Muller, C S Miller, et al.
Leukemia|January 1, 1992
Cancer susceptibility in ataxia-telangiectasiaR D Peterson, J D Funkhouser, C M Tuck-Muller, et al.
Journal of Medical Genetics|January 5, 2002
High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sampleM Ehrlich, F Tsien, D Herrera, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Chromosome studies in 10 patients with the Rett syndromeJ W Moore, C M Tuck-Muller, M Murphy, et al.
American Journal of Medical Genetics|May 17, 1996
A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspringC M Tuck-Muller, M Varela, S Li, et al.
American Journal of Medical Genetics|March 9, 1999
Adrenal insufficiency in Smith-Lemli-Opitz syndromeH C Andersson, J Frentz, J E Martínez, et al.
American Journal of Medical Genetics|June 5, 1995
Translocation 10;18 in a patient with juvenile neuronal ceroid-lipofuscinosis (Batten disease)C M Tuck-Muller, P R Dyken, S Li, et al.
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.
Pageof 4