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American Journal of Medical Genetics
|
February 6, 1999
1p microdeletion in sibs with minimal phenotypic manifestations
J E Martínez, C M Tuck-Muller, W Gasparrini, et al.
Stain Technology
|
September 1, 1984
A method for combined C-banding and silver staining
C 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 media
G H Thomas, C M Tuck-Muller, C S Miller, et al.
Leukemia
|
January 1, 1992
Cancer susceptibility in ataxia-telangiectasia
R 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 sample
M Ehrlich, F Tsien, D Herrera, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1986
Chromosome studies in 10 patients with the Rett syndrome
J 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 offspring
C M Tuck-Muller, M Varela, S Li, et al.
American Journal of Medical Genetics
|
March 9, 1999
Adrenal insufficiency in Smith-Lemli-Opitz syndrome
H 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 daughter
C M Tuck-Muller, J E Martinez, D A Batista, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics
|
February 6, 1999
1p microdeletion in sibs with minimal phenotypic manifestations
J E Martínez, C M Tuck-Muller, W Gasparrini, et al.
Stain Technology
|
September 1, 1984
A method for combined C-banding and silver staining
C 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 media
G H Thomas, C M Tuck-Muller, C S Miller, et al.
Leukemia
|
January 1, 1992
Cancer susceptibility in ataxia-telangiectasia
R 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 sample
M Ehrlich, F Tsien, D Herrera, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1986
Chromosome studies in 10 patients with the Rett syndrome
J 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 offspring
C M Tuck-Muller, M Varela, S Li, et al.
American Journal of Medical Genetics
|
March 9, 1999
Adrenal insufficiency in Smith-Lemli-Opitz syndrome
H 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 daughter
C M Tuck-Muller, J E Martinez, D A Batista, et al.
Page
of 4