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C M Tuck-Muller

Showing results (1-10 of 33) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1987
Autosomal dominant congenital cataract associated with chromosomal translocation [t(3;4)(p26.2;p15)]P D Reese, C M Tuck-Muller, I H Maumenee
Cytogenetics and Cell Genetics|August 31, 2001
The origin of four squirrel monkey cell lines established by karyotype analysisJ G Scammell, J L Wright, C M Tuck-Muller
American Journal of Medical Genetics|August 22, 1997
Hyperlipidemia, insulin-dependent diabetes mellitus, and rapidly progressive diabetic retinopathy and nephropathy in Prader-Willi syndrome with del(15)(q11.2q13)R Bassali, W H Hoffman, H Chen, et al.
Clinical Genetics|April 1, 1993
Fertility and the cri du chat syndromeJ E Martínez, C M Tuck-Muller, D Superneau, et al.
Human Genetics|March 1, 1988
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin geneH Youssoufian, P Chance, C M Tuck-Muller, et al.
American Journal of Medical Genetics|March 27, 1995
Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridizationH Chen, C M Tuck-Muller, D A Batista, et al.
Progress in Clinical and Biological Research|January 1, 1989
Centromere separation and aneuploidy in human mitotic mutants: Roberts syndromeE W Jabs, C M Tuck-Muller, R Cusano, et al.
Cytogenetics and Cell Genetics|January 1, 1984
NOR associations with heterochromatinC M Tuck-Muller, B L Bordson, M Varela, et al.
American Journal of Medical Genetics|January 2, 1995
A rapid method for PCR amplification of DNA directly from cells fixed in Carnoy's fixativeS Li, C M Tuck-Muller, Q Yan, 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.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1987
Autosomal dominant congenital cataract associated with chromosomal translocation [t(3;4)(p26.2;p15)]P D Reese, C M Tuck-Muller, I H Maumenee
Cytogenetics and Cell Genetics|August 31, 2001
The origin of four squirrel monkey cell lines established by karyotype analysisJ G Scammell, J L Wright, C M Tuck-Muller
American Journal of Medical Genetics|August 22, 1997
Hyperlipidemia, insulin-dependent diabetes mellitus, and rapidly progressive diabetic retinopathy and nephropathy in Prader-Willi syndrome with del(15)(q11.2q13)R Bassali, W H Hoffman, H Chen, et al.
Clinical Genetics|April 1, 1993
Fertility and the cri du chat syndromeJ E Martínez, C M Tuck-Muller, D Superneau, et al.
Human Genetics|March 1, 1988
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin geneH Youssoufian, P Chance, C M Tuck-Muller, et al.
American Journal of Medical Genetics|March 27, 1995
Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridizationH Chen, C M Tuck-Muller, D A Batista, et al.
Progress in Clinical and Biological Research|January 1, 1989
Centromere separation and aneuploidy in human mitotic mutants: Roberts syndromeE W Jabs, C M Tuck-Muller, R Cusano, et al.
Cytogenetics and Cell Genetics|January 1, 1984
NOR associations with heterochromatinC M Tuck-Muller, B L Bordson, M Varela, et al.
American Journal of Medical Genetics|January 2, 1995
A rapid method for PCR amplification of DNA directly from cells fixed in Carnoy's fixativeS Li, C M Tuck-Muller, Q Yan, 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.
Pageof 4