Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.

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An unusual case of gastrointestinal bleeding.Bilateral pheochromocytomas, hemihyperplasia, and subtle somatic mosaicism: the importance of detecting low-level uniparental disomy.Age-Related Chromosomal Aberrations in Patients with Diffuse Large B-Cell Lymphoma: An Approach

P2860

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P2860

Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.

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http://www.wikidata.org/entity/Q39764344

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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2011年學術文章

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name

Molecular cytogenetic characte ...... omocytomas and paragangliomas.

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Molecular cytogenetic characte ...... omocytomas and paragangliomas.

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type

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Molecular cytogenetic characte ...... omocytomas and paragangliomas.

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Molecular cytogenetic characte ...... omocytomas and paragangliomas.

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prefLabel

Molecular cytogenetic characte ...... omocytomas and paragangliomas.

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Molecular cytogenetic characte ...... omocytomas and paragangliomas.

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P1476

Molecular cytogenetic characte ...... romocytomas and paragangliomas

@en

P2093

Ales Vicha

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Anna Krepelova

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David Sumerauer

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Marie Jarosova

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Milena Holzerova

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Pavel Prochazka

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Roman Kodet

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Tomas Eckschlager

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P2860

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

Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Pheochromocytoma. Special considerations in children.

Malignant pheochromocytoma: current status and initiatives for future progress.

Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.

Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas.

Genetic differences in endocrine pancreatic tumor subtypes detected by comparative genomic hybridization

Phaeochromocytoma.

P2888

s12253-011-9385-8

P304

801-808

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scholarly article

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10.1007/S12253-011-9385-8

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P478

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Zdenek Musil

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2011-04-05T00:00:00Z

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P698

21461997

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P921

phaeochromocytoma

Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.

about

P2860

P2860

Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.

description

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type

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921