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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 25, 2000
A large 6q deletion is a common cytogenetic alteration in fibroadenomas, pre-malignant lesions, and carcinomas of the breast
M G Tibiletti, F Sessa, B Bernasconi, et al.
International Journal of Cancer
|
June 22, 2000
Genetic progression in microsatellite instability high (MSI-H) colon cancers correlates with clinico-pathological parameters: A study of the TGRbetaRII, BAX, hMSH3, hMSH6, IGFIIR and BLM genes
G A Calin, R Gafà, M G Tibiletti, et al.
Cancer Genetics and Cytogenetics
|
November 11, 1998
Numerical abnormalities of chromosomes 1 and 10 in endometrial adenocarcinoma: fluorescence in situ hybridization analysis of 23 archival paraffin-embedded samples
R Muresu, A Cossu, A M Scarpa, et al.
Clinical Genetics
|
January 26, 2007
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC
A Stella, N C Surdo, P Lastella, et al.
Molecular and Cellular Endocrinology
|
April 25, 2000
Premature ovarian failure
W Vegetti, A Marozzi, E Manfredini, et al.
International Journal of Cancer
|
August 17, 1999
BRCA1 and BRCA2 genes: role in hereditary breast and ovarian cancer in Italy
M Santarosa, R Dolcetti, M D Magri, et al.
International Journal of Cancer
|
June 22, 2000
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
M Miozzo, L Dalprà, P Riva, et al.
Cancer Genetics
|
August 27, 2019
Inherited cancer syndromes in 220 Italian ovarian cancer patients
I Carnevali, C Riva, A M Chiaravalli, et al.
Cancer Research
|
October 1, 1996
Early involvement of 6q in surface epithelial ovarian tumors
M G Tibiletti, B Bernasconi, D Furlan, et al.
Journal of Medical Genetics
|
August 3, 2006
Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region
S Russo, P Finelli, M P Recalcati, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 25, 2000
A large 6q deletion is a common cytogenetic alteration in fibroadenomas, pre-malignant lesions, and carcinomas of the breast
M G Tibiletti, F Sessa, B Bernasconi, et al.
International Journal of Cancer
|
June 22, 2000
Genetic progression in microsatellite instability high (MSI-H) colon cancers correlates with clinico-pathological parameters: A study of the TGRbetaRII, BAX, hMSH3, hMSH6, IGFIIR and BLM genes
G A Calin, R Gafà, M G Tibiletti, et al.
Cancer Genetics and Cytogenetics
|
November 11, 1998
Numerical abnormalities of chromosomes 1 and 10 in endometrial adenocarcinoma: fluorescence in situ hybridization analysis of 23 archival paraffin-embedded samples
R Muresu, A Cossu, A M Scarpa, et al.
Clinical Genetics
|
January 26, 2007
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC
A Stella, N C Surdo, P Lastella, et al.
Molecular and Cellular Endocrinology
|
April 25, 2000
Premature ovarian failure
W Vegetti, A Marozzi, E Manfredini, et al.
International Journal of Cancer
|
August 17, 1999
BRCA1 and BRCA2 genes: role in hereditary breast and ovarian cancer in Italy
M Santarosa, R Dolcetti, M D Magri, et al.
International Journal of Cancer
|
June 22, 2000
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
M Miozzo, L Dalprà, P Riva, et al.
Cancer Genetics
|
August 27, 2019
Inherited cancer syndromes in 220 Italian ovarian cancer patients
I Carnevali, C Riva, A M Chiaravalli, et al.
Cancer Research
|
October 1, 1996
Early involvement of 6q in surface epithelial ovarian tumors
M G Tibiletti, B Bernasconi, D Furlan, et al.
Journal of Medical Genetics
|
August 3, 2006
Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region
S Russo, P Finelli, M P Recalcati, et al.
Page
of 6