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L F Meisner

Showing results (41-50 of 78) with videos related to

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European Journal of Pediatrics|January 18, 1979
Parachute mitral valve, coarctation of aorta, radius aplasia, and omphalocele in an infant with the trisomy 18 syndromeS Ishikawa, E F Gilbert, L F Meisner, et al.
Cancer Research|January 15, 1989
Rare clonal karyotypic variants in primary cultures of human breast carcinoma cellsR Zhang, J Wiley, S P Howard, et al.
Genes, Chromosomes & Cancer|March 1, 1992
Losses of 3p, 11p, and 13q in EJ/ras-transformable simian virus 40-immortalized human uroepithelial cellsC Kao, S Q Wu, M Bhatthacharya, et al.
Genes, Chromosomes & Cancer|July 1, 1993
Use of fluorescence in situ hybridization for retrospective detection of aneuploidy in multiple myelomaW Lee, K Han, R M Drut, et al.
The American Journal of Pathology|July 1, 1993
Use of FISH to detect chromosomal translocations and deletions. Analysis of chromosome rearrangement in synovial sarcoma cells from paraffin-embedded specimensW Lee, K Han, C P Harris, et al.
Lancet (London, England)|September 8, 1973
Microanalysis of chromosomes with x-ray energy dispersionL F Meisner, T W Chuprevich, S L Inhorn, et al.
Lancet (London, England)|February 21, 1976
Letter: Trisomy-20 syndrome in manP D Pallister, J Herrmann, L F Meisner, et al.
American Journal of Medical Genetics|January 1, 1977
The trisomy 4p syndrome: case report and reviewC H Gonzalez, A Sommer, L F Meisner, et al.
American Journal of Medical Genetics. Supplement|January 1, 1987
Newborn infant with del(9)(pter----q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary earsS A Kargas, G A Kargas, S Chandra, et al.
Breast Cancer Research and Treatment|January 1, 1996
FISH detection of HER-2/neu oncogene amplification in early onset breast cancerW R Xing, K W Gilchrist, C P Harris, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
European Journal of Pediatrics|January 18, 1979
Parachute mitral valve, coarctation of aorta, radius aplasia, and omphalocele in an infant with the trisomy 18 syndromeS Ishikawa, E F Gilbert, L F Meisner, et al.
Cancer Research|January 15, 1989
Rare clonal karyotypic variants in primary cultures of human breast carcinoma cellsR Zhang, J Wiley, S P Howard, et al.
Genes, Chromosomes & Cancer|March 1, 1992
Losses of 3p, 11p, and 13q in EJ/ras-transformable simian virus 40-immortalized human uroepithelial cellsC Kao, S Q Wu, M Bhatthacharya, et al.
Genes, Chromosomes & Cancer|July 1, 1993
Use of fluorescence in situ hybridization for retrospective detection of aneuploidy in multiple myelomaW Lee, K Han, R M Drut, et al.
The American Journal of Pathology|July 1, 1993
Use of FISH to detect chromosomal translocations and deletions. Analysis of chromosome rearrangement in synovial sarcoma cells from paraffin-embedded specimensW Lee, K Han, C P Harris, et al.
Lancet (London, England)|September 8, 1973
Microanalysis of chromosomes with x-ray energy dispersionL F Meisner, T W Chuprevich, S L Inhorn, et al.
Lancet (London, England)|February 21, 1976
Letter: Trisomy-20 syndrome in manP D Pallister, J Herrmann, L F Meisner, et al.
American Journal of Medical Genetics|January 1, 1977
The trisomy 4p syndrome: case report and reviewC H Gonzalez, A Sommer, L F Meisner, et al.
American Journal of Medical Genetics. Supplement|January 1, 1987
Newborn infant with del(9)(pter----q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary earsS A Kargas, G A Kargas, S Chandra, et al.
Breast Cancer Research and Treatment|January 1, 1996
FISH detection of HER-2/neu oncogene amplification in early onset breast cancerW R Xing, K W Gilchrist, C P Harris, et al.
Pageof 8