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Human genetics

Showing results (611-620 of 11,264) with videos related to

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Human Genetics|November 1, 1991
Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridizationR Slim, J Weissenbach, V C Nguyen, et al.
Human Genetics|November 1, 1991
Genotypic analysis of families with lactate dehydrogenase A (M) deficiency by selective DNA amplificationM Maekawa, K Sudo, S S Li, et al.
Human Genetics|November 1, 1991
Chromosomal instability in breast cancer patientsL Barrios, M R Caballín, R Miró, et al.
Human Genetics|November 1, 1991
Chromosomal mosaicism: a follow-up study of 39 unselected children found at birthC H Gravholt, U Friedrich, J Nielsen
Human Genetics|November 1, 1991
Hypercholesterolemia in five Israeli Christian-Arab kindreds is caused by the "Lebanese" allele at the low density lipoprotein receptor gene locus and by an additional independent major factorA Oppenheim, Y Friedlander, E J Dann, et al.
Human Genetics|November 1, 1991
A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locusR Fahsold, H D Rott, P Lorenz
Human Genetics|June 1, 1990
Loss of heterozygosity of the L-myc oncogene in human breast tumorsI Bieche, M H Champeme, G Merlo, et al.
Human Genetics|June 1, 1990
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter)T Arinami, T Hirano, K Kobayashi, et al.
Human Genetics|May 18, 2010
Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian childrenDevendra K Amre, David R Mack, Kenneth Morgan, et al.
Human Genetics|April 29, 2010
The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)Delfien Syx, Fransiska Malfait, Lut Van Laer, et al.
Pageof 1,127

Showing results (611-620 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|November 1, 1991
Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridizationR Slim, J Weissenbach, V C Nguyen, et al.
Human Genetics|November 1, 1991
Genotypic analysis of families with lactate dehydrogenase A (M) deficiency by selective DNA amplificationM Maekawa, K Sudo, S S Li, et al.
Human Genetics|November 1, 1991
Chromosomal instability in breast cancer patientsL Barrios, M R Caballín, R Miró, et al.
Human Genetics|November 1, 1991
Chromosomal mosaicism: a follow-up study of 39 unselected children found at birthC H Gravholt, U Friedrich, J Nielsen
Human Genetics|November 1, 1991
Hypercholesterolemia in five Israeli Christian-Arab kindreds is caused by the "Lebanese" allele at the low density lipoprotein receptor gene locus and by an additional independent major factorA Oppenheim, Y Friedlander, E J Dann, et al.
Human Genetics|November 1, 1991
A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locusR Fahsold, H D Rott, P Lorenz
Human Genetics|June 1, 1990
Loss of heterozygosity of the L-myc oncogene in human breast tumorsI Bieche, M H Champeme, G Merlo, et al.
Human Genetics|June 1, 1990
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter)T Arinami, T Hirano, K Kobayashi, et al.
Human Genetics|May 18, 2010
Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian childrenDevendra K Amre, David R Mack, Kenneth Morgan, et al.
Human Genetics|April 29, 2010
The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)Delfien Syx, Fransiska Malfait, Lut Van Laer, et al.
Pageof 1,127