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American Journal of Public Health
|
September 25, 2010
Increased Black-White disparities in mortality after the introduction of lifesaving innovations: a possible consequence of US federal laws
Robert S Levine, George S Rust, Maria Pisu, et al.
Journal of Human Genetics
|
April 6, 2018
QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardation
J Gödiker, M Grüneberg, I DuChesne, et al.
The American Journal of Medicine
|
July 15, 2015
Mammography Screening Among the Elderly: A Research Challenge
Maureen Sanderson, Robert S Levine, Mary K Fadden, et al.
Nature Genetics
|
September 10, 1998
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy
S Rust, M Walter, H Funke, et al.
Molecular Genetics and Metabolism
|
February 7, 2012
Life with too much polyprenol: polyprenol reductase deficiency
J E H Gründahl, Z Guan, S Rust, et al.
Molecular Genetics and Metabolism
|
August 7, 2019
Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England
A Broomfield, J Davison, J Roberts, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 27, 1999
Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred
A T Remaley, S Rust, M Rosier, et al.
Plos One
|
May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
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Search research articles
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Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
American Journal of Public Health
|
September 25, 2010
Increased Black-White disparities in mortality after the introduction of lifesaving innovations: a possible consequence of US federal laws
Robert S Levine, George S Rust, Maria Pisu, et al.
Journal of Human Genetics
|
April 6, 2018
QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardation
J Gödiker, M Grüneberg, I DuChesne, et al.
The American Journal of Medicine
|
July 15, 2015
Mammography Screening Among the Elderly: A Research Challenge
Maureen Sanderson, Robert S Levine, Mary K Fadden, et al.
Nature Genetics
|
September 10, 1998
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy
S Rust, M Walter, H Funke, et al.
Molecular Genetics and Metabolism
|
February 7, 2012
Life with too much polyprenol: polyprenol reductase deficiency
J E H Gründahl, Z Guan, S Rust, et al.
Molecular Genetics and Metabolism
|
August 7, 2019
Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England
A Broomfield, J Davison, J Roberts, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 27, 1999
Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred
A T Remaley, S Rust, M Rosier, et al.
Plos One
|
May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
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of 9