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X-linked mental retardation: in pursuit of a gene map.
scientific article published in June 1993
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scholarly article
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stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
editorial
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title
X-linked mental retardation: in pursuit of a gene map.
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
author name string
Schwartz CE
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
language of work or name
English
0 references
publication date
1 June 1993
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
volume
52
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
issue
6
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
page(s)
1025-1031
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
cites work
Familial sex-linked mental retardation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Linkage mapping of a severe X-linked mental retardation syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked mental retardation: Renpenning revisited
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked mental retardation, macro-orchidism, and the Xq27 fragile site
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
A form of X-linked mental retardation with marfanoid habitus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Conference report: International Workshop on the fragile X and X-linked mental retardation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
A marker X chromosome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Severely retarded children in a London area: prevalence and provision of services
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked mental retardation and-or hydrocephalus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked mental retardation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Allan-Herndon syndrome. I. Clinical studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Gene for non-specific X-linked mental retardation maps in the pericentromeric region.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
XLMR genes: update 1990.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Non-specific X linked mental retardation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
MRX8: an X-linked mental retardation condition with linkage to Xq21.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Nomenclature guidelines for X-linked mental retardation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
XLMR genes: update 1992.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
A second-generation linkage map of the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Linkage to Xq28 in a family with nonspecific X-linked mental retardation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked nonspecific mental retardation:Report of a large kindred
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked mental retardation associated with macro-orchidism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Constitutional chromosomal breakage.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Familial X-linked mental retardation with an X chromosome abnormality
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity--a new syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Marker X chromosomes, mental retardation and macro-orchidism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-Linked Mental Deficiency Megalotestes Syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
X-linked mental retardation with macro-orchidism and marker X chromosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Familial X-linked mental retardation, verbal disability, and marker X chromosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
The X-linked syndrome of macroorchidism and mental retardation: Further observations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
25 May 2018
Sex-linked Microphthalmia and Mental Deficiency.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
Hereditary mental defect showing the pattern of sex influence.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
Fragile X-linked mental retardation: the Martin-Bell syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
X-linked mental retardation: a study of 7 families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
Nonspecific X-linked mental retardation II: the frequency in British Columbia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
Linkage localization of Börjeson-Forssman-Lehmann syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682268
retrieved
15 August 2018
On the gates of hell and a most unusual gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503437
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Monoamine oxidase deficiency in males with an X chromosome deletion
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503437
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
X linked mental retardation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503437
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503437
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1682268
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
PubMed ID
8503437
1 reference
stated in
Europe PubMed Central
PMCID
1682268
retrieved
14 November 2017
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