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Identification and quantitation of benzoxazinoids in wheat malt beer by qNMR and GC–MS

Food science & technology, 2016-01, Vol.65, p.1133-1137

2016

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Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies

PloS one, 2017-02, Vol.12 (2), p.e0171663-e0171663

2017

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Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup

Journal of the American Academy of Dermatology, 2016-02, Vol.74 (2), p.325-332

2016

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Clinical heterogeneity and reduced penetrance in DICER1 syndrome: a report of three families

Tumori, 2021-12, Vol.107 (6), p.NP144-NP148

2021

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Treating secondary malignant neoplasms: A burden of childhood cancer survivors

Tumori, 2023-10, Vol.109 (5), p.436-441

2023

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Cutaneous Melanoma in Childhood and Adolescence Shows Frequent Loss of INK4A and Gain of KIT

Journal of investigative dermatology, 2009-07, Vol.129 (7), p.1759-1768

2009

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Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

Nature genetics, 2020-04, Vol.52 (5), p.494-504

2020

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Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

Scientific reports, 2015-10, Vol.5 (1), p.15454-15454, Article 15454

2015

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A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

BMC medical genetics, 2014-05, Vol.15 (1), p.59-59

2014

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A large de novo9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

BMC medical genetics, 2014-05, Vol.15 (1), Article 59

2014

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Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations

Melanoma research, 2008-12, Vol.18 (6), p.431-437

2008

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Bilateral preaxial polydactyly in a WAGR syndrome patient

American journal of medical genetics. Part A, 2005-05, Vol.134A (4), p.426-429

2005

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Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome

Human genetics, 1996-12, Vol.98 (6), p.646-650

1996

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Bilateral preaxial polydactyly in a WAGR syndrome patient

American journal of medical genetics, 2005, Vol.134A (4), p.426-429

2005

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Bilateral preaxial polydactyly in a WAGR syndrome patient

American Journal of Medical Genetics Part A, 2005, Vol.134A (4), p.426-429

2005

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Identification and quantitation of benzoxazinoids in wheat malt beer by qNMR and GC–MS

Insights into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1

Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup

Analysis of Italian BRCA1/2 Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern Italy

Clinical heterogeneity and reduced penetrance in DICER1 syndrome: a report of three families

Clinical genetic testing for familial melanoma in Italy: A cooperative study

Treating secondary malignant neoplasms: A burden of childhood cancer survivors

Cutaneous Melanoma in Childhood and Adolescence Shows Frequent Loss of INK4A and Gain of KIT

Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

A large de novo9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations

Bilateral preaxial polydactyly in a WAGR syndrome patient

Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome

Bilateral preaxial polydactyly in a WAGR syndrome patient

Bilateral preaxial polydactyly in a WAGR syndrome patient

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