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International Journal of Molecular Sciences
|
June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 25, 2018
Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages
Leigh Jackson, Anita O'Connor, Milena Paneque, et al.
The Oncologist
|
March 30, 2026
Association Between Pathologic Chemotherapy Response Score and Pattern of Recurrence in Advanced High-Grade Serous Ovarian Cancer
Francesco Mezzapesa, Antonio De Leo, Camelia Alexandra Coada, et al.
American Journal of Medical Genetics. Part A
|
January 4, 2026
Low-Level Mosaicism in Tuberous Sclerosis Complex (TSC): Diagnostic and Clinical Implications From Two Novel Cases and Literature Review
Irene Ambrosetti, Carlotta Pia Cristalli, Francesca Montanari, et al.
World Journal of Surgical Oncology
|
May 28, 2026
Bilateral risk reducing mastectomy uptake trends in healthy BRCA1/2 mutation carriers of an European City, the brachoice study
Marco Bernini, Sofia Innocenti, Daniela Turchetti, et al.
Journal of Human Genetics
|
November 11, 2016
Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study
Maria Teresa Ricci, Sara Miccoli, Daniela Turchetti, et al.
Oncotarget
|
February 11, 2017
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype
Roberta Zuntini, Laura Cortesi, Daniele Calistri, et al.
European Journal of Endocrinology
|
January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders
Lucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
BMC Nephrology
|
February 13, 2025
The importance of a multidisciplinary approach in two tricky cases: the perfect match for Fabry disease
Gian Marco Berti, Valeria Aiello, Gisella Vischini, et al.
European Journal of Human Genetics : EJHG
|
September 15, 2020
Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach
Maria Luisa Di Pietro, Drieda Zaçe, Alessia Orfino, et al.
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of 12
Search research articles
Search
Showing results (71-80 of 112) with videos related to
Sort By:
Page
of 12
International Journal of Molecular Sciences
|
June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 25, 2018
Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages
Leigh Jackson, Anita O'Connor, Milena Paneque, et al.
The Oncologist
|
March 30, 2026
Association Between Pathologic Chemotherapy Response Score and Pattern of Recurrence in Advanced High-Grade Serous Ovarian Cancer
Francesco Mezzapesa, Antonio De Leo, Camelia Alexandra Coada, et al.
American Journal of Medical Genetics. Part A
|
January 4, 2026
Low-Level Mosaicism in Tuberous Sclerosis Complex (TSC): Diagnostic and Clinical Implications From Two Novel Cases and Literature Review
Irene Ambrosetti, Carlotta Pia Cristalli, Francesca Montanari, et al.
World Journal of Surgical Oncology
|
May 28, 2026
Bilateral risk reducing mastectomy uptake trends in healthy BRCA1/2 mutation carriers of an European City, the brachoice study
Marco Bernini, Sofia Innocenti, Daniela Turchetti, et al.
Journal of Human Genetics
|
November 11, 2016
Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study
Maria Teresa Ricci, Sara Miccoli, Daniela Turchetti, et al.
Oncotarget
|
February 11, 2017
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype
Roberta Zuntini, Laura Cortesi, Daniele Calistri, et al.
European Journal of Endocrinology
|
January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders
Lucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
BMC Nephrology
|
February 13, 2025
The importance of a multidisciplinary approach in two tricky cases: the perfect match for Fabry disease
Gian Marco Berti, Valeria Aiello, Gisella Vischini, et al.
European Journal of Human Genetics : EJHG
|
September 15, 2020
Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach
Maria Luisa Di Pietro, Drieda Zaçe, Alessia Orfino, et al.
Page
of 12