Bilateral granulosa cell tumors: a novel malignant manifestation of multiple endocrine neoplasia 1 syndrome found in a patient with a rare menin in-frame deletion.

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第一作者： Michael J,Hall

第一单位： Department of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA, USA.

作者： Michael J,Hall ^[1] ; Julie,Innocent ^[2] ; Christina,Rybak ^[1] ; Colleen,Veloski ^[3] ; Walter J,Scott ^[4] ; Hong,Wu ^[5] ; John A,Ridge ^[4] ; John P,Hoffman ^[4] ; Hossein,Borghaei ^[2] ; Aruna,Turaka ^[6] ; Mary B,Daly ^[1]

作者单位： Department of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA, USA. ^[1] Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA. ^[2] Department of Internal Medicine, Fox Chase Cancer Center, Philadelphia, PA, USA. ^[3] Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA. ^[4] Department of Pathology, Fox Chase Cancer Center, Philadelphia, PA, USA. ^[5] Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA. ^[6]

关键词 hyperparathyroidism menin gene ovarian tumors

DOI 10.2147/TACG.S72223

PMID 25733923

发布时间 2020-10-01

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The application of clinical genetics

2015年8卷

69-73页

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Bilateral granulosa cell tumors: a novel malignant manifestation of multiple endocrine neoplasia 1 syndrome found in a patient with a rare menin in-frame deletion.

The application of clinical genetics

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The application of clinical genetics

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Bilateral granulosa cell tumors: a novel malignant manifestation of multiple endocrine neoplasia 1 syndrome found in a patient with a rare menin in-frame deletion.

The application of clinical genetics

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The application of clinical genetics

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