Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1. (Q43104784)

From Wikidata

Jump to navigation Jump to search

scientific article published in December 1997

Language	Label	Description	Also known as
English	Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1.	scientific article published in December 1997

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1. (English)

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

susceptibility locus

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Bennett RL

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Karayiorgou M

2

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Sobin CA

3

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Norwood TH

4

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Kay MA

5

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

language of work or name

0 references

publication date

1 December 1997

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

61

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

6

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

1450-1454

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Dissecting the genetic complexity of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

The genetics of schizophrenia: a current, genetic-epidemiologic perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

A polygenic theory of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Genetic vulnerability to schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Partial trisomy chromosome 5 cosegregating with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Association within a family of a balanced autosomal translocation with major mental illness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Chromosomal aberrations and schizophrenia. Autosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

25 May 2018

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

15 August 2018

The Roscommon Family Study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

15 August 2018

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716062

15 August 2018

Linkage analysis of IL4 and other chromosome 5q31.1 markers and total serum immunoglobulin E concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9399892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9399892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q43104784&oldid=1595727685"