(Q40389355)

20 September 2017

Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH. (English)

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sporadic pheochromocytoma

20 September 2017

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16

Jan P Dumanski

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20 September 2017

9

Henning Dralle

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20 September 2017

Caroline Jarbo

1

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20 September 2017

Patrick G Buckley

2

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20 September 2017

Arkadiusz Piotrowski

3

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20 September 2017

Kiran K Mantripragada

4

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20 September 2017

Magdalena Benetkiewicz

5

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20 September 2017

Teresita Diaz de Ståhl

6

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20 September 2017

Cordelia F Langford

7

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20 September 2017

Simon G Gregory

8

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20 September 2017

Oliver Gimm

10

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20 September 2017

Martin Bäckdahl

11

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20 September 2017

Janos Geli

12

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20 September 2017

Catharina Larsson

13

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20 September 2017

Gunnar Westin

14

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20 September 2017

Göran Akerström

15

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20 September 2017

language of work or name

English

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publication date

1 March 2006

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International Journal of Cancer

20 September 2017

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20 September 2017

118

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20 September 2017

1159-1164

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20 September 2017

5

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Germ-line mutations in nonsyndromic pheochromocytoma

20 September 2017

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

21 January 2018

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Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma

21 January 2018

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Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

21 January 2018

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

21 January 2018

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

21 January 2018

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High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

21 January 2018

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A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

21 January 2018

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Genomic microarrays in the spotlight

21 January 2018

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DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

21 January 2018

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

21 January 2018

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Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray.

21 January 2018

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

21 January 2018

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Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

21 January 2018

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Detection of large-scale variation in the human genome

21 January 2018

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Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas

21 January 2018

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The DNA sequence of human chromosome 22

21 January 2018

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Loss of heterozygosity on long arm of chromosome 22 in sporadic colorectal carcinoma

21 January 2018

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Fine mapping of chromosome 22q tumor suppressor gene candidate regions in astrocytoma.

21 January 2018

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Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.

21 January 2018

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Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases

21 January 2018

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Differential Genetic Alterations in von Hippel-Lindau Syndrome-Associated and Sporadic Pheochromocytomas

21 January 2018

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A novel candidate region linked to development of both pheochromocytoma and head/neck paraganglioma

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/IJC.21385

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release_uanwjqgkzbfhpme5dmufdkznki

20 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/uanwjqgkzbfhpme5dmufdkznki

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference