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Journal of Experimental & Clinical Cancer Research : CR
|
February 15, 2003
Breast MR imaging screening in eight women proved or suspected to be carriers of BRCA1&2 gene mutations
A Cilotti, M A Caligo, G Cipollini, et al.
Thyroid : Official Journal of the American Thyroid Association
|
October 21, 2000
Cyclin D1 overexpression in thyroid carcinomas: relation with clinico-pathological parameters, retinoblastoma gene product, and Ki67 labeling index
F Basolo, M A Caligo, A Pinchera, et al.
Annals of Human Genetics
|
January 25, 2008
Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis
F Marroni, G Cipollini, B Peissel, et al.
Anticancer Research
|
November 1, 1993
Genomic PCR-SSCP analysis of the metastasis associated NM23-H1 (NME1) gene: a study on colorectal cancer
A Bafico, L Varesco, L De Benedetti, et al.
International Journal of Cancer
|
March 16, 1995
NM23 gene expression correlates with cell growth rate and S-phase
M A Caligo, G Cipollini, L Fiore, et al.
British Journal of Cancer
|
July 2, 1999
Microsatellite instability and mismatch repair gene inactivation in sporadic pancreatic and colon tumours
C Ghimenti, P Tannergård, S Wahlberg, et al.
Genes, Chromosomes & Cancer
|
January 1, 1992
The NM23 gene maps to human chromosome band 17q22 and shows a restriction fragment length polymorphism with BglII
L Varesco, M A Caligo, P Simi, et al.
Journal of Endocrinological Investigation
|
February 8, 2024
When to suspect infantile hypercalcemia-1?
A Brancatella, D Cappellani, L Pierotti, et al.
Journal of Endocrinological Investigation
|
May 8, 2020
Disorders of sexual development with XY karyotype and female phenotype: clinical findings and genetic background in a cohort from a single centre
G Costagliola, M Cosci O di Coscio, B Masini, et al.
Journal of Endocrinological Investigation
|
August 10, 2023
Clinical and molecular characteristics of two Italian kindreds with hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome
E Dinoi, L Pierotti, L Mazoni, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 45) with videos related to
Sort By:
Page
of 5
Journal of Experimental & Clinical Cancer Research : CR
|
February 15, 2003
Breast MR imaging screening in eight women proved or suspected to be carriers of BRCA1&2 gene mutations
A Cilotti, M A Caligo, G Cipollini, et al.
Thyroid : Official Journal of the American Thyroid Association
|
October 21, 2000
Cyclin D1 overexpression in thyroid carcinomas: relation with clinico-pathological parameters, retinoblastoma gene product, and Ki67 labeling index
F Basolo, M A Caligo, A Pinchera, et al.
Annals of Human Genetics
|
January 25, 2008
Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis
F Marroni, G Cipollini, B Peissel, et al.
Anticancer Research
|
November 1, 1993
Genomic PCR-SSCP analysis of the metastasis associated NM23-H1 (NME1) gene: a study on colorectal cancer
A Bafico, L Varesco, L De Benedetti, et al.
International Journal of Cancer
|
March 16, 1995
NM23 gene expression correlates with cell growth rate and S-phase
M A Caligo, G Cipollini, L Fiore, et al.
British Journal of Cancer
|
July 2, 1999
Microsatellite instability and mismatch repair gene inactivation in sporadic pancreatic and colon tumours
C Ghimenti, P Tannergård, S Wahlberg, et al.
Genes, Chromosomes & Cancer
|
January 1, 1992
The NM23 gene maps to human chromosome band 17q22 and shows a restriction fragment length polymorphism with BglII
L Varesco, M A Caligo, P Simi, et al.
Journal of Endocrinological Investigation
|
February 8, 2024
When to suspect infantile hypercalcemia-1?
A Brancatella, D Cappellani, L Pierotti, et al.
Journal of Endocrinological Investigation
|
May 8, 2020
Disorders of sexual development with XY karyotype and female phenotype: clinical findings and genetic background in a cohort from a single centre
G Costagliola, M Cosci O di Coscio, B Masini, et al.
Journal of Endocrinological Investigation
|
August 10, 2023
Clinical and molecular characteristics of two Italian kindreds with hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome
E Dinoi, L Pierotti, L Mazoni, et al.
Page
of 5