Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis (Q41133769)

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scientific article published on February 1991

Language	Label	Description	Also known as
English	Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis	scientific article published on February 1991

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

electrophoresis

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Christine Petit

3

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Europe PubMed Central

PubMed publication ID

27 September 2017

author name string

Vincent A

1

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Heitz D

2

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Kretz C

4

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Oberlé I

5

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Mandel JL

6

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

language of work or name

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publication date

1 February 1991

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Europe PubMed Central

PubMed publication ID

27 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

349

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

6310

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

624-626

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Fragile X syndrome: a unique mutation in man.

1 reference

https://api.crossref.org/works/10.1038%2F349624A0

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%2F349624A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

1 reference

https://api.crossref.org/works/10.1038%2F349624A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A new DNA marker tightly linked to the fragile X locus (FRAXA).

1 reference

https://api.crossref.org/works/10.1038%2F349624A0

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%2F349624A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F349624A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage

1 reference

https://api.crossref.org/works/10.1038%2F349624A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A model for the separation of large DNA molecules by crossed field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2F349624A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/349624A0

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 September 2017

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