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Annals of Human Genetics
|
September 1, 1996
Geographic clustering of human Y-chromosome haplotypes
A Ruiz Linares, K Nayar, D B Goldstein, et al.
Clinical Genetics
|
September 27, 2014
The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome
V Shashi, P Xie, K Schoch, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 1999
Microsatellites provide evidence for Y chromosome diversity among the founders of the New World
A Ruiz-Linares, D Ortíz-Barrientos, M Figueroa, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
August 19, 2021
Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?
R Mellis, R Y Eberhardt, S J Hamilton, et al.
Clinical Genetics
|
July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
G Heimer, D Marek-Yagel, E Eyal, et al.
Annals of Human Genetics
|
April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspective
C Capelli, N Redhead, V Romano, et al.
Epilepsy Research
|
November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy
J M Lynch, S K Tate, P Kinirons, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2006
The alpha-synuclein gene in multiple system atrophy
T Ozawa, D G Healy, P M Abou-Sleiman, et al.
Journal of Viral Hepatitis
|
April 14, 2012
Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response
P J Clark, A J Thompson, M Zhu, et al.
Nature
|
April 25, 2014
Guidelines for investigating causality of sequence variants in human disease
D G MacArthur, T A Manolio, D P Dimmock, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 112) with videos related to
Sort By:
Page
of 12
Annals of Human Genetics
|
September 1, 1996
Geographic clustering of human Y-chromosome haplotypes
A Ruiz Linares, K Nayar, D B Goldstein, et al.
Clinical Genetics
|
September 27, 2014
The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome
V Shashi, P Xie, K Schoch, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 1999
Microsatellites provide evidence for Y chromosome diversity among the founders of the New World
A Ruiz-Linares, D Ortíz-Barrientos, M Figueroa, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
August 19, 2021
Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?
R Mellis, R Y Eberhardt, S J Hamilton, et al.
Clinical Genetics
|
July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
G Heimer, D Marek-Yagel, E Eyal, et al.
Annals of Human Genetics
|
April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspective
C Capelli, N Redhead, V Romano, et al.
Epilepsy Research
|
November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy
J M Lynch, S K Tate, P Kinirons, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2006
The alpha-synuclein gene in multiple system atrophy
T Ozawa, D G Healy, P M Abou-Sleiman, et al.
Journal of Viral Hepatitis
|
April 14, 2012
Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response
P J Clark, A J Thompson, M Zhu, et al.
Nature
|
April 25, 2014
Guidelines for investigating causality of sequence variants in human disease
D G MacArthur, T A Manolio, D P Dimmock, et al.
Page
of 12