Germline BRCA2 mutations detected in pediatric sequencing studies impact parents' evaluation and care.

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Germline BRCA2 mutations detected in pediatric sequencing studies impact parents' evaluation and care.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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Germline BRCA2 mutations detec ...... parents' evaluation and care.

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Germline BRCA2 mutations detec ...... parents' evaluation and care.

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Germline BRCA2 mutations detec ...... parents' evaluation and care.

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Germline BRCA2 mutations detec ...... parents' evaluation and care.

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Germline BRCA2 mutations detec ...... parents' evaluation and care.

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Germline BRCA2 mutations detec ...... parents' evaluation and care.

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P1476

Germline BRCA2 mutations detec ...... parents' evaluation and care.

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Alex Kentsis

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Andrew L Kung

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Brian H Kushner

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Jacob Musinsky

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Jennifer Kennedy

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Megan Harlan

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Michael F Walsh

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Neerav Shukla

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Paul Meyers

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Stephen Roberts

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P2860

A map of human genome variation from population-scale sequencing

A global reference for human genetic variation

The Fanconi anaemia/BRCA pathway

ClinVar: public archive of interpretations of clinically relevant variants

Biallelic inactivation of BRCA2 in Fanconi anemia

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.

Increased cancer risks for relatives of very early-onset breast cancer cases with and without BRCA1 and BRCA2 mutations.

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer.

Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype

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scholarly article

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10.1101/MCS.A001925

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P478

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Kenneth Offit

Mark Robson

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2017-06-27T00:00:00Z

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28655807

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5701310

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