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H Ledbetter

Showing results (151-160 of 388) with videos related to

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American Journal of Human Genetics|April 1, 1990
Five polymorphic microsatellite VNTRs on the human X chromosomeJ A Luty, Z Guo, H F Willard, et al.
American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.
American Journal of Human Genetics|May 6, 2004
Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriagesAnthony J Schaeffer, June Chung, Konstantina Heretis, et al.
Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.
Genome Research|August 1, 1996
Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical regionY Ning, A Roschke, S L Christian, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1981
In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase proteinD W Melton, D S Konecki, D H Ledbetter, et al.
American Journal of Medical Genetics|December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomyV Tonk, R A Schultz, S L Christian, et al.
Nature Genetics|May 1, 1997
Methylation-specific PCR simplifies imprinting analysisT Kubota, S Das, S L Christian, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicismDaniela Bettio, Erin L Baldwin, Romeo Carrozzo, 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.
Pageof 39

Showing results (151-160 of 388) with videos related to

Sort By:
Pageof 39
American Journal of Human Genetics|April 1, 1990
Five polymorphic microsatellite VNTRs on the human X chromosomeJ A Luty, Z Guo, H F Willard, et al.
American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.
American Journal of Human Genetics|May 6, 2004
Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriagesAnthony J Schaeffer, June Chung, Konstantina Heretis, et al.
Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.
Genome Research|August 1, 1996
Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical regionY Ning, A Roschke, S L Christian, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1981
In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase proteinD W Melton, D S Konecki, D H Ledbetter, et al.
American Journal of Medical Genetics|December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomyV Tonk, R A Schultz, S L Christian, et al.
Nature Genetics|May 1, 1997
Methylation-specific PCR simplifies imprinting analysisT Kubota, S Das, S L Christian, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicismDaniela Bettio, Erin L Baldwin, Romeo Carrozzo, 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.
Pageof 39