Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Ledbetter

Showing results (171-180 of 388) with videos related to

Pageof 39
Sort By:
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.
American Journal of Medical Genetics|January 1, 1987
The Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome: male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal cardiac defectF Greenberg, M V Gresik, R J Carpenter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
American College of Medical Genetics statement of diagnostic testing for uniparental disomyL G Shaffer, N Agan, J D Goldberg, et al.
Genes, Chromosomes & Cancer|March 1, 1994
Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markersM Isomura, A Tanigami, H Saito, et al.
Oncogene|January 1, 1987
Localization of myeloperoxidase to the long arm of human chromosome 17: relationship to the 15; 17 translocation of acute promyelocytic leukemiaP van Tuinen, K R Johnson, S A Ledbetter, et al.
Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1991
Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4Y Ning, J L Weber, A M Killary, et al.
American Journal of Human Genetics|January 1, 1997
Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardationA C Wong, Y Ning, J Flint, et al.
Pageof 39

Showing results (171-180 of 388) with videos related to

Sort By:
Pageof 39
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.
American Journal of Medical Genetics|January 1, 1987
The Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome: male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal cardiac defectF Greenberg, M V Gresik, R J Carpenter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
American College of Medical Genetics statement of diagnostic testing for uniparental disomyL G Shaffer, N Agan, J D Goldberg, et al.
Genes, Chromosomes & Cancer|March 1, 1994
Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markersM Isomura, A Tanigami, H Saito, et al.
Oncogene|January 1, 1987
Localization of myeloperoxidase to the long arm of human chromosome 17: relationship to the 15; 17 translocation of acute promyelocytic leukemiaP van Tuinen, K R Johnson, S A Ledbetter, et al.
Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1991
Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4Y Ning, J L Weber, A M Killary, et al.
American Journal of Human Genetics|January 1, 1997
Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardationA C Wong, Y Ning, J Flint, et al.
Pageof 39