(Q52077161)

English

Implications of fragile X expression in normal males for the nature of the mutation.

scientific article published in November 1986

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

Implications of fragile X expression in normal males for the nature of the mutation. (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

author name string

Ledbetter DH

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

Ledbetter SA

2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

Nussbaum RL

3

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

language of work or name

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publication date

1 November 1986

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

324

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

6093

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

161-163

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

https://scigraph.springernature.com/pub.10.1038/324161a0

0 references

Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Caffeine enhances fragile (X) expression in somatic cell hybrids

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of fragile X chromosome in human-rodent somatic cell hybrids.

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

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

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic linkage heterogeneity in the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Constitutive fragile sites and cancer.

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical implications and classification of the constitutive fragile sites

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Fragile sites: overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expression

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

The effect of caffeine on fragile X expression

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

On the gates of hell and a most unusual gene

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2F324161A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/324161A0

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3785381

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