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Biochemical and Biophysical Research Communications
|
July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations
S Kemp, M J Ligtenberg, B M van Geel, et al.
Intensive Care Medicine
|
February 8, 2000
Pharmacokinetics of cefpirome in critically ill patients with renal failure treated by continuous veno-venous hemofiltration
T S Van der Werf, J W Fijen, N C Van de Merbel, et al.
Clinical Chemistry
|
February 20, 2010
Interlaboratory diagnostic validation of conformation-sensitive capillary electrophoresis for mutation scanning
Christopher J Mattocks, Gemma Watkins, Daniel Ward, et al.
Genes, Chromosomes & Cancer
|
April 3, 2001
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)
M J Eleveld, D Bodmer, G Merkx, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 12, 2004
[18F]Fluoro-2-deoxy-D-glucose positron emission tomography detects gastric carcinoma in an early stage in an asymptomatic E-cadherin mutation carrier
Mariette C A van Kouwen, Joost P H Drenth, Wim J G Oyen, et al.
Breast Cancer Research and Treatment
|
February 3, 2011
A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patients
M A Didraga, E H van Beers, S A Joosse, et al.
American Journal of Human Genetics
|
June 19, 1998
An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation
D Bodmer, M J Eleveld, M J Ligtenberg, et al.
Breast Cancer Research and Treatment
|
August 16, 2008
Prediction of BRCA1-association in hereditary non-BRCA1/2 breast carcinomas with array-CGH
Simon A Joosse, Erik H van Beers, Ivon H G Tielen, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2013
The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype
Chau-To Kwok, Ingrid P Vogelaar, Wendy A van Zelst-Stams, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
November 8, 2019
Two types of primary mucinous ovarian tumors can be distinguished based on their origin
Michiel Simons, Femke Simmer, Johan Bulten, et al.
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of 14
Search research articles
Search
Showing results (111-120 of 136) with videos related to
Sort By:
Page
of 14
Biochemical and Biophysical Research Communications
|
July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations
S Kemp, M J Ligtenberg, B M van Geel, et al.
Intensive Care Medicine
|
February 8, 2000
Pharmacokinetics of cefpirome in critically ill patients with renal failure treated by continuous veno-venous hemofiltration
T S Van der Werf, J W Fijen, N C Van de Merbel, et al.
Clinical Chemistry
|
February 20, 2010
Interlaboratory diagnostic validation of conformation-sensitive capillary electrophoresis for mutation scanning
Christopher J Mattocks, Gemma Watkins, Daniel Ward, et al.
Genes, Chromosomes & Cancer
|
April 3, 2001
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)
M J Eleveld, D Bodmer, G Merkx, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 12, 2004
[18F]Fluoro-2-deoxy-D-glucose positron emission tomography detects gastric carcinoma in an early stage in an asymptomatic E-cadherin mutation carrier
Mariette C A van Kouwen, Joost P H Drenth, Wim J G Oyen, et al.
Breast Cancer Research and Treatment
|
February 3, 2011
A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patients
M A Didraga, E H van Beers, S A Joosse, et al.
American Journal of Human Genetics
|
June 19, 1998
An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation
D Bodmer, M J Eleveld, M J Ligtenberg, et al.
Breast Cancer Research and Treatment
|
August 16, 2008
Prediction of BRCA1-association in hereditary non-BRCA1/2 breast carcinomas with array-CGH
Simon A Joosse, Erik H van Beers, Ivon H G Tielen, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2013
The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype
Chau-To Kwok, Ingrid P Vogelaar, Wendy A van Zelst-Stams, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
November 8, 2019
Two types of primary mucinous ovarian tumors can be distinguished based on their origin
Michiel Simons, Femke Simmer, Johan Bulten, et al.
Page
of 14