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The Journal of Clinical Endocrinology and Metabolism
|
June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumors
M J Ligtenberg, M Siers, A P Themmen, et al.
British Journal of Cancer
|
February 24, 2006
Surveillance of women at high risk for hereditary ovarian cancer is inefficient
A L Oei, L F Massuger, J Bulten, et al.
British Journal of Cancer
|
December 8, 2005
A multiplex PCR predictor for aCGH success of FFPE samples
E H van Beers, S A Joosse, M J Ligtenberg, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1993
Control of antigenic variation in African trypanosomes
P Borst, J H Gommers-Ampt, M J Ligtenberg, et al.
Human Mutation
|
January 1, 1995
Two intronic mutations in the adrenoleukodystrophy gene
S Kemp, M J Ligtenberg, B M van Geel, et al.
Virchows Archiv : an International Journal of Pathology
|
April 10, 2010
Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial
L I Overbeek, R P Hermens, J H van Krieken, et al.
Human Genetics
|
July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation
A F van Lieburg, M A Verdijk, F Schoute, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 15, 1993
Episialin (MUC1) inhibits cytotoxic lymphocyte-target cell interaction
E van de Wiel-van Kemenade, M J Ligtenberg, A J de Boer, et al.
Human Reproduction (Oxford, England)
|
October 2, 1998
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene
J H Tuerlings, M J Ligtenberg, J A Kremer, et al.
American Journal of Human Genetics
|
May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region
M Wijker, M J Ligtenberg, F Schoute, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
The Journal of Clinical Endocrinology and Metabolism
|
June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumors
M J Ligtenberg, M Siers, A P Themmen, et al.
British Journal of Cancer
|
February 24, 2006
Surveillance of women at high risk for hereditary ovarian cancer is inefficient
A L Oei, L F Massuger, J Bulten, et al.
British Journal of Cancer
|
December 8, 2005
A multiplex PCR predictor for aCGH success of FFPE samples
E H van Beers, S A Joosse, M J Ligtenberg, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1993
Control of antigenic variation in African trypanosomes
P Borst, J H Gommers-Ampt, M J Ligtenberg, et al.
Human Mutation
|
January 1, 1995
Two intronic mutations in the adrenoleukodystrophy gene
S Kemp, M J Ligtenberg, B M van Geel, et al.
Virchows Archiv : an International Journal of Pathology
|
April 10, 2010
Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial
L I Overbeek, R P Hermens, J H van Krieken, et al.
Human Genetics
|
July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation
A F van Lieburg, M A Verdijk, F Schoute, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 15, 1993
Episialin (MUC1) inhibits cytotoxic lymphocyte-target cell interaction
E van de Wiel-van Kemenade, M J Ligtenberg, A J de Boer, et al.
Human Reproduction (Oxford, England)
|
October 2, 1998
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene
J H Tuerlings, M J Ligtenberg, J A Kremer, et al.
American Journal of Human Genetics
|
May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region
M Wijker, M J Ligtenberg, F Schoute, et al.
Page
of 3