(Q24671075)

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X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism (English)

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

borderline personality disorder

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18 January 2019

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author name string

Brunner HG

1

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Europe PubMed Central

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13 October 2019

Nelen MR

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

van Zandvoort P

3

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Europe PubMed Central

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13 October 2019

Abeling NG

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

van Gennip AH

5

1 reference

Europe PubMed Central

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13 October 2019

Wolters EC

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Kuiper MA

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Ropers HH

8

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

van Oost BA

9

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Europe PubMed Central

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13 October 2019

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publication date

1 June 1993

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Europe PubMed Central

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13 October 2019

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

52

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13 October 2019

6

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Europe PubMed Central

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13 October 2019

1032-1039

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Human monoamine oxidase A gene determines levels of enzyme activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

7 April 2017

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

7 April 2017

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

7 April 2017

Norrie disease resulting from a gene deletion: clinical features and DNA studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Dinucleotide repeat polymorphism at the MAOA locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Monoamines and abnormal behaviour. A multi-aminergic perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Structure of the human gene for monoamine oxidase type A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

XLMR genes: update 1992.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Isolation and characterization of a candidate gene for Norrie disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Isolation of a candidate gene for Norrie disease by positional cloning

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Aggression in humans correlates with cerebrospinal fluid amine metabolites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Cerebrospinal fluid monoamine metabolite levels in male arsonists

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 September 2017

Assay of platelet monoamine oxidase in whole blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Conceptualizing a serotonin trait. A behavioral dimension of constraint.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Marked amine and amine metabolite changes in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Serotonergic dysfunction and aggression control.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Multipoint linkage analysis of DXS369 and DXS304 in fragile X families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Gene for non-specific X-linked mental retardation maps in the pericentromeric region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Cerebrospinal fluid monoamine metabolites, aggression, and impulsivity in disruptive behavior disorders of children and adolescents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Three dinucleotide repeat polymorphisms at the DXS178 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

30 May 2018

Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682278

28 November 2018

Simultaneous determination of catecholamines and metanephrines in urine by HPLC with fluorometric detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/8503438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

More on monoamine oxidase activity in whole blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/8503438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8503438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monoamine oxidase deficiency in males with an X chromosome deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/8503438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous determination of acidic 3,4-dihydroxyphenylalanine metabolites and 5-hydroxyindole-3-acetic acid in urine by high-performance liquid chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/8503438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503438%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

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