(Q35281112)

7 August 2017

1 reference

title

Chromosomal aberrations and schizophrenia. Autosomes (English)

1 reference

7 August 2017

1 reference

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1393302

21 September 2022

author name string

A. S. Bassett

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1393302

21 September 2022

language of work or name

English

0 references

publication date

1 September 1992

1 reference

full work available at URL

7 August 2017

https://europepmc.org/articles/PMC3188307

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1393302

https://europepmc.org/articles/PMC3188307?pdf=render

21 September 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1393302

British Journal of Psychiatry

21 September 2022

published in

1 reference

7 August 2017

161

1 reference

7 August 2017

323-334

1 reference

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

The incidence of minor physical anomalies in adult male schizophrenics.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

The inheritance of schizophrenia spectrum disorders: a reanalysis of the Danish adoptee study data

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Pericentric inversions. Problems and significance for clinical genetics

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Ring chromosome 18 in mother and daughter

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

D-D translocations in patients with mental illness.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Psychiatric illness in first-degree relatives of schizophrenic and surgical control patients. A family study using DSM-III criteria.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Fragile 19p13 in a family with mental illness.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Intrachromosomal insertion of chromosome 13 in a family with psychosis and mental subnormality.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Down's syndrome and Alzheimer's disease: a review

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Partial trisomy chromosome 5 cosegregating with schizophrenia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Evidence that the gene for tuberous sclerosis is on chromosome 9

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Strategies for linkage studies of schizophrenia: pedigrees, DNA markers, and statistical analyses

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Schizophrenia and mental handicap: an historical review, with implications for further research

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Mapping genes for manic-depression and schizophrenia with DNA markers

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Linkage strategies for genetically complex traits. I. Multilocus models

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Genomic imprinting: review and relevance to human diseases.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

A cytogenetic study of children with psychiatric disorders

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Schizophrenia and organic brain syndrome with trisomy 8 (group-C trisomy 8 [47, XX, 8+])

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Trisomy 8 syndrome. A psychological and somatic study of a mentally non-retarded male with 46,XY/47,XY,+8 chromosome constitution.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Retinoblastoma and Subband Deletion of Chromosome 13

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Dementia in ageing mental defectives: a clinical and neuropathological study

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Trisomy 8. Report of a mosaic human male with near-normal phenotype and normal IQ, ascertained through infertility.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Genetic disorders presenting as ?schizophrenia?. Karl bonhoeffer's early view of the psychoses in the light of medical genetics

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

No linkage of chromosome 5q11-q13 markers to schizophrenia in Scottish families

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

A balanced chromosomal translocation partially co-segregating with psychotic illness in a family

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188307

Sex chromosomes and psychosis. The case for a pseudoautosomal locus

26 September 2018

1 reference

12 December 2020

Chromosome 5 and schizophrenia: implications for genetic linkage studies

1 reference

12 December 2020

Paranoid schizophrenia in a mongoloid defective: some theoretical considerations derived from an unusual case

1 reference

12 December 2020

Familial manic-depressive illness with deleted short arm of chromosome 21: coincidental or causal?

1 reference

12 December 2020

18p- syndrome. A further case

1 reference

12 December 2020

XXY syndrome XY XO mosaicism and acentric chromosomal fragments in male schizophrenics

1 reference

12 December 2020

Chromosomal translocation t(2;18)(q21;q23) in a schizophrenic individual and his daughter

1 reference

12 December 2020

Mosaicism and the trisomy 8 syndrome

1 reference

12 December 2020

A new heritable fragile site on human chromosome 3

1 reference

12 December 2020

CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN

1 reference

12 December 2020

Chromosome aberrations in patients with paranoid psychosis

1 reference

12 December 2020

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

1 reference

12 December 2020

A folate sensitive heritable fragile site at 19p13

1 reference

12 December 2020

Down's syndrome with mania

1 reference

12 December 2020

Human chromosome banding specific for electron microscopy

1 reference

12 December 2020

Localization of a susceptibility locus for schizophrenia on chromosome 5

1 reference

12 December 2020

Minor physical anomalies in schizophrenia

1 reference

12 December 2020

Identifiers

DOI

10.1192/BJP.161.3.323

1 reference

7 August 2017

1 reference

7 August 2017

1 reference