(Q33594985)

English

Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain? (English)

1 reference

Europe PubMed Central

28 July 2017

0 references

susceptibility locus

1 reference

based on heuristic

inferred from title

Becker muscular dystrophy

1 reference

based on heuristic

inferred from title

1

object named as

Zatz M

1 reference

Europe PubMed Central

28 July 2017

object named as

Vallada H

2

0 references

author name string

Melo MS

3

1 reference

Europe PubMed Central

28 July 2017

Passos-Bueno MR

4

1 reference

Europe PubMed Central

28 July 2017

Vieira AH

5

1 reference

Europe PubMed Central

28 July 2017

Vainzof M

6

1 reference

Europe PubMed Central

28 July 2017

Gill M

7

1 reference

Europe PubMed Central

28 July 2017

Gentil V

8

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 February 1993

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

28 July 2017

30

1 reference

Europe PubMed Central

28 July 2017

131-134

1 reference

Europe PubMed Central

28 July 2017

2

1 reference

Europe PubMed Central

28 July 2017

Behavioral and personality correlates of epilepsy: a review, methodological critique, and conceptual model.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

The genetics of schizophrenic and schizoid disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Psychiatric disability in female carriers of the fragile X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Major genes for major affective disorder?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Evidence for a sex chromosome locus for schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Social class, marriage, and fertility in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Concordance by sex in sibling pairs with schizophrenia is paternally inherited. Evidence for a pseudoautosomal locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Exclusion of a schizophrenia susceptibility gene from the chromosome 5q11-q13 region: new data and a reanalysis of previous reports

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

A family with Alport syndrome and psychosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Nature of the genetic contribution to psychotic illness--a continuum viewpoint

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

[A case of Becker muscular dystrophy with schizophrenic symptoms]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in progressive muscular dystrophies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

28 July 2018

The monogenic theory of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

Investigation on genetic heterogeneity in Duchenne muscular dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

Dystrophin gene transcribed from different promoters in neuronal and glial cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

Evidence against linkage of schizophrenia to chromosome 5q11-q13 markers in systematically ascertained families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016270

30 October 2018

Heritability of schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family history study of schizophrenia-related personality disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Splitting schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a susceptibility locus for schizophrenia on chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence for linkage between chromosome 5 markers and schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unsound methodology in investigating a pseudoautosomal locus in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8445617

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.30.2.131

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

ResearchGate publication ID

0 references

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