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I Hansmann

Showing results (121-130 of 129) with videos related to

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Progress in Clinical and Biological Research|January 1, 1990
Transgenic mouse--an in vivo system for detection of aneugensA T Natarajan, S E Vlasblom, A Manca, et al.
American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.
Cancer Genetics and Cytogenetics|May 30, 2002
Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemiaV J Picos-Cárdenas, J P Meza-Espinoza, M Gutiérrez-Angulo, et al.
American Journal of Human Genetics|January 1, 1993
A genetic map of chromosome 20q12-q13.1: multiple highly polymorphic microsatellite and RFLP markers linked to the maturity-onset diabetes of the young (MODY) locusC B Rothschild, G Akots, R Hayworth, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Report of the First International Workshop on Human Chromosome 20 Mapping 1993C L Smith, T Keith, I Hansmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Molecular structure and chromosomal mapping of the human homolog of the agouti geneH Y Kwon, S J Bultman, C Löffler, et al.
Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.
American Journal of Medical Genetics|January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literatureP Steinbach, W N Adkins, H Caspar, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Pageof 13

Showing results (121-130 of 129) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 129 results.
Progress in Clinical and Biological Research|January 1, 1990
Transgenic mouse--an in vivo system for detection of aneugensA T Natarajan, S E Vlasblom, A Manca, et al.
American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.
Cancer Genetics and Cytogenetics|May 30, 2002
Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemiaV J Picos-Cárdenas, J P Meza-Espinoza, M Gutiérrez-Angulo, et al.
American Journal of Human Genetics|January 1, 1993
A genetic map of chromosome 20q12-q13.1: multiple highly polymorphic microsatellite and RFLP markers linked to the maturity-onset diabetes of the young (MODY) locusC B Rothschild, G Akots, R Hayworth, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Report of the First International Workshop on Human Chromosome 20 Mapping 1993C L Smith, T Keith, I Hansmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Molecular structure and chromosomal mapping of the human homolog of the agouti geneH Y Kwon, S J Bultman, C Löffler, et al.
Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.
American Journal of Medical Genetics|January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literatureP Steinbach, W N Adkins, H Caspar, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Pageof 13