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 (Q36593274)

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scientific article published on October 1, 1982

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English	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	scientific article published on October 1, 1982

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

R. Brookwell

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6215863

30 August 2023

A. Daniel

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6215863

30 August 2023

G. Turner

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6215863

30 August 2023

J. Fishburn

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6215863

30 August 2023

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6215863

30 August 2023

publication date

1 October 1982

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320130206

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320130206

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

13

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

139-148

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Inherited congenital normofunctional testicular hyperplasia and mental deficiency

1

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

Journal de genetique humaine

2

19

137

author name string

Escalante

publication date

1971

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

Familial X-linked mental retardation with an X chromosome abnormality

4

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

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

5

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

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

6

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

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

7

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

Fragile X-linked mental retardation

8

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

Chromosome banding required for studies on X-linked mental retardation

10

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

12

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

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

13

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

14

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

X-linked mental retardation associated with macro-orchidism

16

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

The New England Journal of Medicine

17

299

1472

author name string

Turner

publication date

1978

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

X-linked mental retardation

18

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

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

19

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

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

20

1 reference

10.1002/AJMG.1320130206

https://api.crossref.org/works/10.1002/AJMG.1320130206

30 August 2023

Identifiers

10.1002/AJMG.1320130206

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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