(Q35124129)

6 August 2017

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

1 reference

6 August 2017

1 reference

B C McGillivray

1

1 reference

6 August 2017

A S Bassett

2

1 reference

6 August 2017

S Langlois

3

1 reference

6 August 2017

T Pantzar

4

1 reference

6 August 2017

S Wood

5

1 reference

6 August 2017

1 January 1990

1 reference

American Journal of Medical Genetics Part A

6 August 2017

1 reference

6 August 2017

35

1 reference

6 August 2017

1

1 reference

6 August 2017

10-13

1 reference

Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5

6 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

The transmission of schizophrenia under a multifactorial threshold model

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

Segregation analysis of schizophrenia and related disorders

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

A polygenic theory of schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

Partial trisomy chromosome 5 cosegregating with schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

Bipolar affective disorders linked to DNA markers on chromosome 11

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

The gene for familial polyposis coli maps to the long arm of chromosome 5.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3142272

Evidence for localization of the gene for hexosaminidase B to the cen leads to q13 region of human chromosome 5 using mouse x human hybrid cells

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1967903

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1967903

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Regional localization of α-galactosidase ( GLA ) to Xpter→q22, hexosaminidase B ( HEXB ) to 5q13→qter, and arylsulfatase B ( ARSB ) to5pter→q13

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1967903

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.1320350103

1 reference

6 August 2017

1 reference

6 August 2017

1 reference