Search research articles
Contact Us
Filters
Showing results (291-300 of 391) with videos related to
Page
of 40
Sort By:
The Science of the Total Environment
|
November 22, 2023
Inferring hospital admissions from SARS-CoV-2 virus loads in wastewater in The Netherlands, August 2020 - February 2022
Wouter A Hetebrij, Ana Maria de Roda Husman, Erwin Nagelkerke, et al.
Genomics
|
May 15, 1997
Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3
R H Giles, F Petrij, H G Dauwerse, et al.
Clinical Genetics
|
July 19, 2012
An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection
Y Hilhorst-Hofstee, A J H A Scholte, M E B Rijlaarsdam, et al.
American Journal of Human Genetics
|
August 1, 1997
Spectrum of mutations in the Batten disease gene, CLN3
P B Munroe, H M Mitchison, A M O'Rawe, et al.
Genomics
|
February 12, 1998
Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease
A Odermatt, P E Taschner, S W Scherer, et al.
Journal of the American Society of Nephrology : JASN
|
October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKD
York Pei, James Obaji, Annie Dupuis, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 8, 2006
A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor
M J E Walenkamp, H J van der Kamp, A M Pereira, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 12, 2010
The jumping SHOX gene--crossover in the pseudoautosomal region resulting in unusual inheritance of Leri-Weill dyschondrosteosis
Sarina G Kant, Hetty J van der Kamp, Marjolein Kriek, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 22, 2010
Pkd1-inactivation in vascular smooth muscle cells and adaptation to hypertension
Sabrine Hassane, Nanna Claij, Martine Jodar, et al.
European Journal of Human Genetics : EJHG
|
April 30, 2015
LRP5 variants may contribute to ADPKD
Wybrich R Cnossen, René H M te Morsche, Alexander Hoischen, et al.
Page
of 40
Search research articles
Search
Showing results (291-300 of 391) with videos related to
Sort By:
Page
of 40
The Science of the Total Environment
|
November 22, 2023
Inferring hospital admissions from SARS-CoV-2 virus loads in wastewater in The Netherlands, August 2020 - February 2022
Wouter A Hetebrij, Ana Maria de Roda Husman, Erwin Nagelkerke, et al.
Genomics
|
May 15, 1997
Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3
R H Giles, F Petrij, H G Dauwerse, et al.
Clinical Genetics
|
July 19, 2012
An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection
Y Hilhorst-Hofstee, A J H A Scholte, M E B Rijlaarsdam, et al.
American Journal of Human Genetics
|
August 1, 1997
Spectrum of mutations in the Batten disease gene, CLN3
P B Munroe, H M Mitchison, A M O'Rawe, et al.
Genomics
|
February 12, 1998
Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease
A Odermatt, P E Taschner, S W Scherer, et al.
Journal of the American Society of Nephrology : JASN
|
October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKD
York Pei, James Obaji, Annie Dupuis, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 8, 2006
A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor
M J E Walenkamp, H J van der Kamp, A M Pereira, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 12, 2010
The jumping SHOX gene--crossover in the pseudoautosomal region resulting in unusual inheritance of Leri-Weill dyschondrosteosis
Sarina G Kant, Hetty J van der Kamp, Marjolein Kriek, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 22, 2010
Pkd1-inactivation in vascular smooth muscle cells and adaptation to hypertension
Sabrine Hassane, Nanna Claij, Martine Jodar, et al.
European Journal of Human Genetics : EJHG
|
April 30, 2015
LRP5 variants may contribute to ADPKD
Wybrich R Cnossen, René H M te Morsche, Alexander Hoischen, et al.
Page
of 40