(Q27694653)

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Impact of NGS in the medical sciences: Genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies

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Impact of NGS in the medical sciences: genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies

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scholarly article

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Impact of NGS in the medical sciences: Genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies (English)

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Impact of NGS in the medical sciences: genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies (English)

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Victor Martínez-Glez

object named as

Víctor Martínez-Glez

6

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author name string

Lapunzina P

1

1 reference

López RO

2

1 reference

Rodríguez-Laguna L

3

1 reference

García-Miguel P

4

1 reference

Martínez AR

5

1 reference

Martínez-Glez V

6

1 reference

Pablo Lapunzina

1

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Rocío Ortiz López

2

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Lara Rodríguez-Laguna

3

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Purificación García-Miguel

4

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Augusto Rojas Martínez

5

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publication date

March 2014

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2014

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Genetics and Molecular Biology

1 reference

37

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1 Suppl

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1 suppl 1

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241-9

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241-249

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Developmental disease and cancer: biological and clinical overlaps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

Exome sequencing identifies the cause of a mendelian disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

Massively parallel sequencing: the next big thing in genetic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

STRING 8--a global view on proteins and their functional interactions in 630 organisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

PIK3CA-Related Segmental Overgrowth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

Germline mutations in HRAS proto-oncogene cause Costello syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

20 March 2017

Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

24 May 2017

Update on pediatric cancer predisposition syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

29 September 2017

Mosaic RASopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

29 September 2017

Rare hereditary diseases with defects in DNA-repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

29 September 2017

Tuberous sclerosis complex: tumors and tumorigenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

29 September 2017

When overgrowth bumps into cancer: the PTEN-opathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3983588

27 November 2018

When Overgrowth Bumps Into Cancer: The PTEN-Opathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/24764758

12 December 2020

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10.1590/S1415-47572014000200010

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PubMed publication ID

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