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D H Ledbetter

Showing results (121-130 of 251) with videos related to

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Nature Genetics|May 1, 1997
Methylation-specific PCR simplifies imprinting analysisT Kubota, S Das, S L Christian, et al.
Experimental Cell Research|January 1, 1991
Tumor suppression by chromosome 11 is not due to cellular senescenceY Ning, J W Shay, M Lovell, et al.
Biochemical and Biophysical Research Communications|November 27, 1985
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2L Chan, P VanTuinen, D H Ledbetter, et al.
Nucleic Acids Research|July 11, 1988
RFLPs revealed by cosmid 131 [HGM9 no. D17S78]J Luty, S Kondoleon, P van Tuinen, et al.
American Journal of Medical Genetics|September 25, 1995
Detection of a subtle rearrangement of chromosome 22 using molecular techniquesL G Biesecker, M Rosenberg, L Dziadzio, et al.
Journal of Virology|November 1, 1988
Structural analysis of a hepatitis B virus genome integrated into chromosome 17p of a human hepatocellular carcinomaY Z Zhou, B L Slagle, L A Donehower, et al.
American Journal of Medical Genetics|April 1, 1986
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17F Greenberg, R F Stratton, L H Lockhart, et al.
The Journal of Pediatrics|April 1, 1983
Miller-Dieker syndrome: lissencephaly and monosomy 17pW B Dobyns, R F Stratton, J T Parke, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
American Journal of Human Genetics|June 1, 1988
Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6F D Ledley, M R Lumetta, H Y Zoghbi, et al.
Pageof 26

Showing results (121-130 of 251) with videos related to

Sort By:
Pageof 26
Nature Genetics|May 1, 1997
Methylation-specific PCR simplifies imprinting analysisT Kubota, S Das, S L Christian, et al.
Experimental Cell Research|January 1, 1991
Tumor suppression by chromosome 11 is not due to cellular senescenceY Ning, J W Shay, M Lovell, et al.
Biochemical and Biophysical Research Communications|November 27, 1985
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2L Chan, P VanTuinen, D H Ledbetter, et al.
Nucleic Acids Research|July 11, 1988
RFLPs revealed by cosmid 131 [HGM9 no. D17S78]J Luty, S Kondoleon, P van Tuinen, et al.
American Journal of Medical Genetics|September 25, 1995
Detection of a subtle rearrangement of chromosome 22 using molecular techniquesL G Biesecker, M Rosenberg, L Dziadzio, et al.
Journal of Virology|November 1, 1988
Structural analysis of a hepatitis B virus genome integrated into chromosome 17p of a human hepatocellular carcinomaY Z Zhou, B L Slagle, L A Donehower, et al.
American Journal of Medical Genetics|April 1, 1986
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17F Greenberg, R F Stratton, L H Lockhart, et al.
The Journal of Pediatrics|April 1, 1983
Miller-Dieker syndrome: lissencephaly and monosomy 17pW B Dobyns, R F Stratton, J T Parke, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
American Journal of Human Genetics|June 1, 1988
Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6F D Ledley, M R Lumetta, H Y Zoghbi, et al.
Pageof 26