(Q40167416)

18 September 2017

1 reference

title

Marker (X)-linked mental retardation (English)

1 reference

18 September 2017

Marker (X)-Linked Mental Retardation (English)

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

8 October 2023

author name string

G. Turner

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6362362

8 October 2023

P. Jacobs

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6362362

8 October 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6362362

8 October 2023

publication date

1 January 1983

1 reference

full work available at URL

18 September 2017

http://link.springer.com/content/pdf/10.1007/978-1-4615-8342-4_2.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

Advances in human genetics

8 October 2023

published in

1 reference

18 September 2017

volume

13

1 reference

18 September 2017

page(s)

83-112

1 reference

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

18 September 2017

cites work

3

1 reference

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Inherited congenital normofunctional testicular hyperplasia and mental deficiency

8 October 2023

4

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

5

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

8 October 2023

11

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

A simple method to demonstrate the fragile X chromosome in fibroblasts

8 October 2023

12

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

X-linked mental retardation: Renpenning revisited

8 October 2023

13

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

Constitutional chromosomal breakage.

8 October 2023

14

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

Familial X-linked mental retardation with an X chromosome abnormality

8 October 2023

16

1 reference

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

8 October 2023

17

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

18

1 reference

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

8 October 2023

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

8 October 2023

20

1 reference

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Feasibility of fragile X chromosome prenatal diagnosis demonstrated

8 October 2023

22

1 reference

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

8 October 2023

23

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

Complex Segregation Analysis with Pointers

8 October 2023

25

1 reference

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A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

8 October 2023

31

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

32

1 reference

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

8 October 2023

39

1 reference

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The Martin-Bell-Renpenning syndrome.

8 October 2023

40

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

X-Linked Mental Deficiency Megalotestes Syndrome

8 October 2023

41

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

PRIMARY AND SECONDARY SEXUAL CHARACTERISTICS

8 October 2023

42

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

44

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

46

1 reference

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

8 October 2023

48

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

Marker X chromosome induction in fibroblasts by FUdR

8 October 2023

49

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

X-linked mental retardation.

8 October 2023

51

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

X-linked mental retardation associated with macro-orchidism

8 October 2023

53

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

The New England Journal of Medicine

8 October 2023

54

299

1472

G Turner

1978

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

55

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

56

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

58

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

59

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

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

8 October 2023

60

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8342-4_2

8 October 2023

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6362362

8 October 2023

1 reference