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Human Genetics
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March 30, 2017
Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA)
Zhe Wang, Ani Manichukal, David C Goff, et al.
Human Genetics
|
May 1, 1988
Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitor
B Bardoni, M Sampietro, M Romano, et al.
Human Genetics
|
April 29, 2014
Determining causality and consequence of expression quantitative trait loci
A Battle, S B Montgomery
Human Genetics
|
February 28, 2014
A human rights approach to an international code of conduct for genomic and clinical data sharing
Bartha M Knoppers, Jennifer R Harris, Isabelle Budin-Ljøsne, et al.
Human Genetics
|
March 6, 2017
The study of human Y chromosome variation through ancient DNA
Toomas Kivisild
Human Genetics
|
February 1, 1988
The molecular basis of HbH disease in Taiwan
H W Peng, S H Han, T Y Chow, et al.
Human Genetics
|
March 12, 2017
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
Christel Depienne, Caroline Nava, Boris Keren, et al.
Human Genetics
|
February 19, 2017
Emerging genotype-phenotype relationships in patients with large NF1 deletions
Hildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N Cooper
Human Genetics
|
March 15, 2017
Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine
Iana H Haralambieva, Inna G Ovsyannikova, Richard B Kennedy, et al.
Human Genetics
|
November 1, 1987
Chromosomal insertion of human papillomavirus 18 sequences in HeLa cells detected by nonisotopic in situ hybridization and reflection contrast microscopy
P F Ambros, H I Karlic
Page
of 957
Search research articles
Search
Showing results (961-970 of 9,569) with videos related to
Sort By:
Page
of 957
Human Genetics
|
March 30, 2017
Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA)
Zhe Wang, Ani Manichukal, David C Goff, et al.
Human Genetics
|
May 1, 1988
Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitor
B Bardoni, M Sampietro, M Romano, et al.
Human Genetics
|
April 29, 2014
Determining causality and consequence of expression quantitative trait loci
A Battle, S B Montgomery
Human Genetics
|
February 28, 2014
A human rights approach to an international code of conduct for genomic and clinical data sharing
Bartha M Knoppers, Jennifer R Harris, Isabelle Budin-Ljøsne, et al.
Human Genetics
|
March 6, 2017
The study of human Y chromosome variation through ancient DNA
Toomas Kivisild
Human Genetics
|
February 1, 1988
The molecular basis of HbH disease in Taiwan
H W Peng, S H Han, T Y Chow, et al.
Human Genetics
|
March 12, 2017
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
Christel Depienne, Caroline Nava, Boris Keren, et al.
Human Genetics
|
February 19, 2017
Emerging genotype-phenotype relationships in patients with large NF1 deletions
Hildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N Cooper
Human Genetics
|
March 15, 2017
Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine
Iana H Haralambieva, Inna G Ovsyannikova, Richard B Kennedy, et al.
Human Genetics
|
November 1, 1987
Chromosomal insertion of human papillomavirus 18 sequences in HeLa cells detected by nonisotopic in situ hybridization and reflection contrast microscopy
P F Ambros, H I Karlic
Page
of 957