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American Journal of Medical Genetics
|
January 30, 1995
Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies
S Shankman, A B Spurdle, D Morris, et al.
Carcinogenesis
|
April 27, 2001
No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer
A B Spurdle, P M Webb, D M Purdie, et al.
Carcinogenesis
|
February 13, 2001
Polymorphisms at the glutathione S-transferase GSTM1, GSTT1 and GSTP1 loci: risk of ovarian cancer by histological subtype
A B Spurdle, P M Webb, D M Purdie, et al.
Molecular Carcinogenesis
|
March 20, 2001
The microsomal epoxide hydrolase Tyr113His polymorphism: association with risk of ovarian cancer
A B Spurdle, D M Purdie, P M Webb, et al.
Cancer Causes & Control : CCC
|
December 12, 2019
Dietary inflammatory index, risk and survival among women with endometrial cancer
C M Nagle, T Ibiebele, N Shivappa, et al.
Hereditary Cancer in Clinical Practice
|
May 3, 2016
Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group
C H H Kerkhofs, A B Spurdle, P J Lindsey, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
September 2, 1999
Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg
J G Kromberg, A Krause, A B Spurdle, et al.
International Journal of Cancer
|
August 5, 2000
Androgen receptor exon 1 CAG repeat length and risk of ovarian cancer
A B Spurdle, P M Webb, X Chen, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
July 9, 2015
BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance
D M Eccles, G Mitchell, A N A Monteiro, et al.
British Journal of Cancer
|
February 9, 2005
Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals
C R Jekimovs, X Chen, J Arnold, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 42) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics
|
January 30, 1995
Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies
S Shankman, A B Spurdle, D Morris, et al.
Carcinogenesis
|
April 27, 2001
No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer
A B Spurdle, P M Webb, D M Purdie, et al.
Carcinogenesis
|
February 13, 2001
Polymorphisms at the glutathione S-transferase GSTM1, GSTT1 and GSTP1 loci: risk of ovarian cancer by histological subtype
A B Spurdle, P M Webb, D M Purdie, et al.
Molecular Carcinogenesis
|
March 20, 2001
The microsomal epoxide hydrolase Tyr113His polymorphism: association with risk of ovarian cancer
A B Spurdle, D M Purdie, P M Webb, et al.
Cancer Causes & Control : CCC
|
December 12, 2019
Dietary inflammatory index, risk and survival among women with endometrial cancer
C M Nagle, T Ibiebele, N Shivappa, et al.
Hereditary Cancer in Clinical Practice
|
May 3, 2016
Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group
C H H Kerkhofs, A B Spurdle, P J Lindsey, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
September 2, 1999
Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg
J G Kromberg, A Krause, A B Spurdle, et al.
International Journal of Cancer
|
August 5, 2000
Androgen receptor exon 1 CAG repeat length and risk of ovarian cancer
A B Spurdle, P M Webb, X Chen, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
July 9, 2015
BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance
D M Eccles, G Mitchell, A N A Monteiro, et al.
British Journal of Cancer
|
February 9, 2005
Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals
C R Jekimovs, X Chen, J Arnold, et al.
Page
of 5