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Genetics Research
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January 13, 2015
FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and the general population display distinct distribution patterns
Yael Laitman, Liat Ries-Levavi, Michal Berkensdadt, et al.
Genetics Research
|
September 15, 2015
The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disorders
Tony Shen, Ariel Lee, Carol Shen, et al.
Genetics Research
|
June 29, 2016
FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile
Lorena Santa María, Solange Aliaga, Víctor Faundes, et al.
Genetics Research
|
September 23, 2015
Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization
Avinash M Veerappa, Raviraj V Suresh, Sangeetha Vishweswaraiah, et al.
Genetics Research
|
September 23, 2015
Next generation sequencing for newborn screening: are we there yet?
Eitan Friedman
Genetics Research
|
March 6, 2018
Association of tribbles homologue 1 gene expression in human umbilical vein endothelial cells with duration of intrauterine exposure to hyperglycaemia
Polina V Popova, Liudmila B Vasileva, Alexandra S Tkachuk, et al.
Genetics Research
|
February 2, 2018
DNA methylation is not involved in dietary restriction induced lifespan extension in adult Drosophila
Ting Lian, Uma Gaur, Q I Wu, et al.
Genetics Research
|
April 28, 2009
A study on the mapping of quantitative trait loci in advanced populations derived from two inbred lines
Chen-Hung Kao, Miao-Hui Zeng
Genetics Research
|
October 9, 2008
Intra-individual and intra-species heterogeneity in nuclear rDNA ITS region of Vigna species from subgenus Ceratotropis
Ajay Saini, Sreenivasulu K Reddy, Narendra Jawali
Genetics Research
|
October 9, 2008
Extreme value theory in analysis of differential expression in microarrays where either only up- or down-regulated genes are relevant or expected
Renata Ivanek, Yrjö T Gröhn, Martin T Wells, et al.
Page
of 50
Search research articles
Search
Showing results (411-420 of 499) with videos related to
Sort By:
Page
of 50
Genetics Research
|
January 13, 2015
FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and the general population display distinct distribution patterns
Yael Laitman, Liat Ries-Levavi, Michal Berkensdadt, et al.
Genetics Research
|
September 15, 2015
The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disorders
Tony Shen, Ariel Lee, Carol Shen, et al.
Genetics Research
|
June 29, 2016
FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile
Lorena Santa María, Solange Aliaga, Víctor Faundes, et al.
Genetics Research
|
September 23, 2015
Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization
Avinash M Veerappa, Raviraj V Suresh, Sangeetha Vishweswaraiah, et al.
Genetics Research
|
September 23, 2015
Next generation sequencing for newborn screening: are we there yet?
Eitan Friedman
Genetics Research
|
March 6, 2018
Association of tribbles homologue 1 gene expression in human umbilical vein endothelial cells with duration of intrauterine exposure to hyperglycaemia
Polina V Popova, Liudmila B Vasileva, Alexandra S Tkachuk, et al.
Genetics Research
|
February 2, 2018
DNA methylation is not involved in dietary restriction induced lifespan extension in adult Drosophila
Ting Lian, Uma Gaur, Q I Wu, et al.
Genetics Research
|
April 28, 2009
A study on the mapping of quantitative trait loci in advanced populations derived from two inbred lines
Chen-Hung Kao, Miao-Hui Zeng
Genetics Research
|
October 9, 2008
Intra-individual and intra-species heterogeneity in nuclear rDNA ITS region of Vigna species from subgenus Ceratotropis
Ajay Saini, Sreenivasulu K Reddy, Narendra Jawali
Genetics Research
|
October 9, 2008
Extreme value theory in analysis of differential expression in microarrays where either only up- or down-regulated genes are relevant or expected
Renata Ivanek, Yrjö T Gröhn, Martin T Wells, et al.
Page
of 50