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Subcutaneous melanocytoma mimicking a lipoma: a rare presentation of a rare neoplasm with histological, immunohistochemical, cytogenetic and molecular characterization.
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- Journal of Cutaneous Pathology, 2016, v. 43, n. 12, p. 1186, doi. 10.1111/cup.12808
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- Article
Diagnosis and management of the phenotypic spectrum of twins with Beckwith‐Wiedemann syndrome.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 7, p. 1139, doi. 10.1002/ajmg.a.61164
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- Article
Update on molecular diagnosis of hereditary hemorrhagic telangiectasia.
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- Human Genetics, 2010, v. 128, n. 1, p. 61, doi. 10.1007/s00439-010-0825-4
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- Article
Phosphorylation of pRb: mechanism for RB pathway inactivation in MYCN-amplified retinoblastoma.
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- Cancer Medicine, 2017, v. 6, n. 3, p. 619, doi. 10.1002/cam4.1010
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- Article
Molecular diagnosis of somatic overgrowth conditions: A single‐center experience.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 3, p. N.PAG, doi. 10.1002/mgg3.536
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- Article
Enhanced Sensitivity for Detection of Low-Level Germline Mosaic RB1 Mutations in Sporadic Retinoblastoma Cases Using Deep Semiconductor Sequencing.
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- Human Mutation, 2014, v. 35, n. 3, p. 384, doi. 10.1002/humu.22488
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- Article