Double Heterozygosity for BRCA1 Pathogenic Variant and BRCA2 Polymorphic Stop Codon K3326X: A Case Report in a Southern Italian Family.

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Double Heterozygosity for BRCA1 Pathogenic Variant and BRCA2 Polymorphic Stop Codon K3326X: A Case Report in a Southern Italian Family.

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2018 nî lūn-bûn

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2018年学术文章

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Double Heterozygosity for BRCA ...... in a Southern Italian Family.

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Double Heterozygosity for BRCA ...... in a Southern Italian Family.

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Double Heterozygosity for BRCA ...... in a Southern Italian Family.

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Double Heterozygosity for BRCA ...... in a Southern Italian Family.

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Double Heterozygosity for BRCA ...... in a Southern Italian Family.

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Double Heterozygosity for BRCA ...... in a Southern Italian Family.

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P1476

Double Heterozygosity for BRCA ...... t in a Southern Italian Family

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P2093

Angela Cardascia

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Davide Quaresmini

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Erica Silvestris

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Franco Silvestris

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P2860

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Five recurrent BRCA1/2 mutations are responsible for cancer predisposition in the majority of Slovenian breast cancer families.

Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability.

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.

Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2.

Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish population.

Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.

New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing

Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.

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scholarly article

case report

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10.3390/IJMS19010285

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English

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Domenica Lovero

Raffaele Palmirotta

Luigia Stefania Stucci

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2018-01-18T00:00:00Z

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29346284

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5796231

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