(Q33620294)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19617690%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1. (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19617690%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

0 references

Ana Cristina Krepischi

1

1 reference

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2 February 2020

Karen Temple

3

1 reference

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2 February 2020

Paulo A Otto

8

1 reference

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2 February 2020

Carla Rosenberg

11

1 reference

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2 February 2020

author name string

D Rajan

2

1 reference

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2 February 2020

V Shrubb

4

1 reference

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2 February 2020

J A Crolla

5

1 reference

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2 February 2020

S Huang

6

1 reference

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2 February 2020

S Beal

7

1 reference

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2 February 2020

N P Carter

9

1 reference

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2 February 2020

A M Vianna-Morgante

10

1 reference

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2 February 2020

publication date

14 July 2009

1 reference

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Cytogenetics and Genome Research

2 February 2020

published in

1 reference

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2 February 2020

volume

125

1 reference

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2 February 2020

issue

1

1 reference

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2 February 2020

page(s)

1-7

1 reference

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Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome

2 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Ligand binding mode of GABAA receptor-associated protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

G-protein pathway suppressor 2 (GPS2) interacts with the regulatory factor X4 variant 3 (RFX4_v3) and functions as a transcriptional co-activator

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Suppressors of hedgehog signaling: Linking aberrant development of neural progenitors and tumorigenesis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

E6AP-dependent degradation of DLG4/PSD95 by high-risk human papillomavirus type 18 E6 protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Hedgehog checkpoints in medulloblastoma: the chromosome 17p deletion paradigm.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Chromosome 17p deletion in human medulloblastoma: a missing checkpoint in the Hedgehog pathway

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

REN: a novel, developmentally regulated gene that promotes neural cell differentiation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

AMF1 (GPS2) modulates p53 transactivation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

The role of p53 in human cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Associations between congenital malformations and childhood cancer. A register-based case-control study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Cancer risk in children with birth defects and in their families: a population based cohort study of 5.2 million children from Norway and Sweden

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

PSD-95 regulates synaptic transmission and plasticity in rat cerebral cortex

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813804

Supernumerary nipples and urologic malignancies

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19617690

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital abnormalities and childhood cancer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19617690

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1159/000218743

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19617690%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19617690%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

PubMed publication ID

19617690

1 reference