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Nederlands Tijdschrift Voor Geneeskunde
|
September 17, 2015
[Maturity-onset diabetes of the young]
Karin van der Tuin, Sabine E Hannema, E C A M Mieke Houdijk, et al.
Kidney International
|
April 14, 1999
Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin
F T van der Loop, L A Monnens, C H Schröder, et al.
Blood
|
November 15, 1993
A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo
B A van der Reijden, J G Dauwerse, J W Wessels, et al.
European Journal of Medical Genetics
|
June 13, 2008
A 400kb duplication, 2.4Mb triplication and 130kb duplication of 9q34.3 in a patient with severe mental retardation
Antoinet C J Gijsbers, Emilia K Bijlsma, Marjan M Weiss, et al.
Genomics
|
July 15, 1997
The human gene ZFP161 on 18p11.21-pter encodes a putative c-myc repressor and is homologous to murine Zfp161 (Chr 17) and Zfp161-rs1 (X Chr)
I Sobek-Klocke, C Disqué-Kochem, M Ronsiek, et al.
Molecular Ecology
|
September 16, 2011
Meta-barcoding of 'dirt' DNA from soil reflects vertebrate biodiversity
Kenneth Andersen, Karen Lise Bird, Morten Rasmussen, et al.
Human Molecular Genetics
|
November 7, 2000
Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells
M S Scheffers, P van der Bent, F Prins, et al.
Lancet (London, England)
|
December 12, 1987
Improved early diagnosis of adult polycystic kidney disease with flanking DNA markers
M H Breuning, S T Reeders, H Brunner, et al.
Blood Cells, Molecules & Diseases
|
November 29, 2007
A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patients
Dorine W Swinkels, Hanka Venselaar, Erwin T Wiegerinck, et al.
Kidney International
|
December 1, 2004
Comparison between siblings and twins supports a role for modifier genes in ADPKD
Alexandre Persu, Michel Duyme, Yves Pirson, et al.
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of 40
Search research articles
Search
Showing results (201-210 of 391) with videos related to
Sort By:
Page
of 40
Nederlands Tijdschrift Voor Geneeskunde
|
September 17, 2015
[Maturity-onset diabetes of the young]
Karin van der Tuin, Sabine E Hannema, E C A M Mieke Houdijk, et al.
Kidney International
|
April 14, 1999
Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin
F T van der Loop, L A Monnens, C H Schröder, et al.
Blood
|
November 15, 1993
A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo
B A van der Reijden, J G Dauwerse, J W Wessels, et al.
European Journal of Medical Genetics
|
June 13, 2008
A 400kb duplication, 2.4Mb triplication and 130kb duplication of 9q34.3 in a patient with severe mental retardation
Antoinet C J Gijsbers, Emilia K Bijlsma, Marjan M Weiss, et al.
Genomics
|
July 15, 1997
The human gene ZFP161 on 18p11.21-pter encodes a putative c-myc repressor and is homologous to murine Zfp161 (Chr 17) and Zfp161-rs1 (X Chr)
I Sobek-Klocke, C Disqué-Kochem, M Ronsiek, et al.
Molecular Ecology
|
September 16, 2011
Meta-barcoding of 'dirt' DNA from soil reflects vertebrate biodiversity
Kenneth Andersen, Karen Lise Bird, Morten Rasmussen, et al.
Human Molecular Genetics
|
November 7, 2000
Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells
M S Scheffers, P van der Bent, F Prins, et al.
Lancet (London, England)
|
December 12, 1987
Improved early diagnosis of adult polycystic kidney disease with flanking DNA markers
M H Breuning, S T Reeders, H Brunner, et al.
Blood Cells, Molecules & Diseases
|
November 29, 2007
A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patients
Dorine W Swinkels, Hanka Venselaar, Erwin T Wiegerinck, et al.
Kidney International
|
December 1, 2004
Comparison between siblings and twins supports a role for modifier genes in ADPKD
Alexandre Persu, Michel Duyme, Yves Pirson, et al.
Page
of 40