(Q50304255)

2 March 2018

title

Brief report: translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia. (English)

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2 March 2018

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C T Gordon

1

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2 March 2018

D Krasnewich

2

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2 March 2018

B White

3

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2 March 2018

M Lenane

4

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2 March 2018

J L Rapoport

5

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2 March 2018

language of work or name

English

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publication date

1 August 1994

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2 March 2018

Journal of Autism and Developmental Disorders

published in

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2 March 2018

volume

24

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2 March 2018

page(s)

537-545

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2 March 2018

issue

4

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2 March 2018

https://scigraph.springernature.com/pub.10.1007/bf02172134

exact match

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cites work

Neurobiologic antecedents of schizophrenia in children. Evidence for an inherited, congenital neurointegrative defect.

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

Infants at risk for schizophrenia: sequelae of a genetic neurointegrative defect. A review and replication analysis of pandysmaturation in the Jerusalem Infant Development Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

Autistic children who become schizophrenic.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

Exclusion of linkage between schizophrenia and the D2 dopamine receptor gene region of chromosome 11q in 112 Irish multiplex families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

Prediction of adult-onset schizophrenia from childhood home movies of the patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

A linkage study of chromosome 11q in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

Pseudoautosomal Locus for Schizophrenia Excluded in 12 Pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02172134

Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.

21 January 2018

1 reference

12 December 2020

Genes, gene map, gene mapping

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12 December 2020

Symptom development in childhood onset schizophrenia

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12 December 2020

Comorbid association of autism and schizophrenia.

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12 December 2020

High Resolution of Human Chromosomes

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12 December 2020

Chromosomal mosaicisms and occasional acentric chromosomal fragments in schizophrenic patients

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12 December 2020

Age at onset and causes of disease

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12 December 2020

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

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12 December 2020

Phenomenology and classification of the childhood psychoses

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12 December 2020

Linkage analysis of schizophrenia: challenges and promise.

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12 December 2020

The phenomenology of schizophrenia occurring in childhood.

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12 December 2020

The genetic epidemiology of schizophrenia and the design of linkage studies

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12 December 2020

Maternal diabetes: the risk for specific birth defects

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12 December 2020

Microdeletion syndromes, balanced translocations, and gene mapping

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12 December 2020

Reverse genetics and human disease

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12 December 2020

Partial trisomy chromosome 5 cosegregating with schizophrenia

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12 December 2020

A complex chromosome rearrangement in a boy with autism.

1 reference

12 December 2020

Cytogenetic studies of males with schizophrenia. Screening for the fragile X chromosome and other chromosomal abnormalities

1 reference

12 December 2020

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families

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12 December 2020

Identifiers

DOI

10.1007/BF02172134

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2 March 2018

PubMed ID

7961336

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2 March 2018