Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.

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http://www.wikidata.org/entity/Q38801071

description

2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

@zh-hant

2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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name

Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.

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type

Item

label

Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.

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prefLabel

Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.

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P1476

Routine genetic screening with a multi-gene panel in patients with pheochromocytomas

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P2093

Aparna Pal

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Ashley B Grossman

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Bahram Jafar-Mohammadi

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Brian Shine

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Greg Sadler

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Treena Cranston

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P2860

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

Identification of the von Hippel-Lindau disease tumor suppressor gene

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

Pheochromocytoma: evaluation, diagnosis, and treatment.

P2888

s12020-017-1310-9

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175-182

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scholarly article

P356

10.1007/S12020-017-1310-9

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Andrea M. Isidori

Radu Mihai

E Sbardella

P577

2017-05-05T00:00:00Z

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P698

28477304

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P921

phaeochromocytoma