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The fragile X chromosome.
scientific article published on January 1983
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Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
review article
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Europe PubMed Central
title
The fragile X chromosome
(English)
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Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
author name string
G R Sutherland
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
language of work or name
English
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publication date
1 January 1983
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Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
published in
International Review of Cytology
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stated in
Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
volume
81
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Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
page(s)
107-143
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
cites work
A fragile secondary constriction on chromosome 2 in five patients with different clinical features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
The X-linked syndrome of macroorchidism and mental retardation: Further observations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of fragile X syndrome with autism
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
Inherited congenital normofunctional testicular hyperplasia and mental deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited congenital normofunctional testicular hyperplasia and mental deficiency. A corroborative study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
Fragile X in a normal male: a cautionary tale
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inborn errors of folate metabolism (first of two parts).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
Basic morphological data of external genitals in 177 healthy central European men
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A simple method to demonstrate the fragile X chromosome in fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation: Renpenning revisited
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X chromosome: consistent demonstration of fragile site in fibroblast cultures
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation and an X-chromosome marker.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutional chromosomal breakage.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Can nutritional supplements help mentally retarded children? an exploratory study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The fragile X chromosome: Current methods
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonspecific X-linked mental retardation I: a review with information from 24 new families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
Nonspecific X-linked mental retardation II: the frequency in British Columbia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
Further delineation of X-linked mental retardation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mental retardation, marker X chromosomes, and silver-staining (NORs)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavior of chromosome cores at heritable fragile sites: 16q22 and Xq27
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation with macro-orchidism and marker X chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation: a study of 7 families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Feasibility of fragile X chromosome prenatal diagnosis demonstrated
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X-linked mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is the fragile X syndrome amenable to treatment?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome banding required for studies on X-linked mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
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inferred from DOI database lookup
A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation with macro-orchidism and marker-X chromosomes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Selective endoreduplication or branched chromosome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marker X syndrome in an oriental family with probable transmission by a normal male.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-Linked Mental Deficiency Megalotestes Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Demonstration of a heritable fragile site in human chromosome 16 with distamycin A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE METHYL FOLATE TRAP A physiological response in man to prevent methyl group deficiency in kwashiorkor (methionine deficiency) and an explanation for folic-acid-induced exacerbation of subacute combined degeneration in pernicious anaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The fragile site on chromosome 16 (q21q22). Data on four new families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile site long arm chromosome 16
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New technique for distinguishing between human chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heritable fragile sites on human chromosomes. IV. Silver staining
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic length of a human chromosomal segment measured by recombination between two fragile sites
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marker X chromosome induction in fibroblasts by FUdR
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked mental retardation, macro-orchidism, and the Xq27 fragile site
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmission of fragile (X) (q27) site from a male
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis of Martin-Bell syndrome associated with fragile site at Xq27-28
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0074-7696(08)62336-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
PubMed publication ID
6347931
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6347931
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
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