The fragile X chromosome. (Q40153740)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

review article

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title

The fragile X chromosome (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

G R Sutherland

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

language of work or name

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1 January 1983

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

International Review of Cytology

10 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

volume

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

page(s)

107-143

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

A fragile secondary constriction on chromosome 2 in five patients with different clinical features

10 October 2019

cites work

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7 January 2021

The X-linked syndrome of macroorchidism and mental retardation: Further observations

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7 January 2021

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

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7 January 2021

Association of fragile X syndrome with autism

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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)

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7 January 2021

Inherited congenital normofunctional testicular hyperplasia and mental deficiency

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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Inherited congenital normofunctional testicular hyperplasia and mental deficiency. A corroborative study

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Fragile X in a normal male: a cautionary tale

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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Inborn errors of folate metabolism (first of two parts).

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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Basic morphological data of external genitals in 177 healthy central European men

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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

A simple method to demonstrate the fragile X chromosome in fibroblasts

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7 January 2021

X-linked mental retardation: Renpenning revisited

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7 January 2021

Fragile X chromosome: consistent demonstration of fragile site in fibroblast cultures

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7 January 2021

X-linked mental retardation and an X-chromosome marker.

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7 January 2021

Constitutional chromosomal breakage.

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7 January 2021

Can nutritional supplements help mentally retarded children? an exploratory study.

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7 January 2021

The fragile X chromosome: Current methods

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Nonspecific X-linked mental retardation I: a review with information from 24 new families

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Nonspecific X-linked mental retardation II: the frequency in British Columbia.

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7 January 2021

Further delineation of X-linked mental retardation.

1 reference

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7 January 2021

Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Mental retardation, marker X chromosomes, and silver-staining (NORs)

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Behavior of chromosome cores at heritable fragile sites: 16q22 and Xq27

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation with macro-orchidism and marker X chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation: a study of 7 families.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Feasibility of fragile X chromosome prenatal diagnosis demonstrated

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Fragile X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Is the fragile X syndrome amenable to treatment?

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Chromosome banding required for studies on X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation with macro-orchidism and marker-X chromosomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Selective endoreduplication or branched chromosome?

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Marker X syndrome in an oriental family with probable transmission by a normal male.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-Linked Mental Deficiency Megalotestes Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Demonstration of a heritable fragile site in human chromosome 16 with distamycin A

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

The fragile site on chromosome 16 (q21q22). Data on four new families

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Fragile site long arm chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

New technique for distinguishing between human chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Heritable fragile sites on human chromosomes. IV. Silver staining

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Genetic length of a human chromosomal segment measured by recombination between two fragile sites

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Marker X chromosome induction in fibroblasts by FUdR

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Transmission of fragile (X) (q27) site from a male

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Prenatal diagnosis of Martin-Bell syndrome associated with fragile site at Xq27-28

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962336-0

7 January 2021

10.1016/S0074-7696(08)62336-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6347931%20AND%20SRC:MED&resulttype=core&format=json