(Q51011951)

27 March 2018

title

Population based prenatal screening for the fragile X syndrome. (English)

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27 March 2018

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G E Palomaki

1

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27 March 2018

publication date

1 January 1994

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27 March 2018

Journal of Medical Screening

published in

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27 March 2018

volume

1

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27 March 2018

issue

1

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27 March 2018

page(s)

65-72

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27 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

The marker (X) syndrome: a cytogenetic and genetic analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

The polymerase chain reaction. A new method of using molecular genetics for medical diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Fragile X screening program in New York State.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Methylation and mutation patterns in the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Couple screening for cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Population screening for fragile X

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

Population screening for fragile-X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096914139400100112

10.1177/096914139400100112

21 January 2018

Identifiers

DOI

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27 March 2018

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27 March 2018