Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male (Q45863462)

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scientific article published in December 1983

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Language	Label	Description	Also known as
English	Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male	scientific article published in December 1983

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

title

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

main subject

hemophilia

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hemophilia B

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author name string

Camerino G

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

Mattei MG

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

Mattei JF

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

Jaye M

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

Mandel JL

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

language of work or name

English

0 references

publication date

1 December 1983

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

published in

Nature

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

volume

306

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

issue

5944

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

page(s)

701-704

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

cites work

Nonspecific X-linked mental retardation--a review

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

High resolution banding and the locus of the Xq fragile site

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked mental retardation with the fragile X. A study of 15 families

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Brief report: linkage between G6PD and fragile-X syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Transmission of fragile (X)(q27) from normal male(s)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of a human anti-haemophilic factor IX cDNA clone using a unique 52-base synthetic oligonucleotide probe deduced from the amino acid sequence of bovine factor IX.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragil (X)(q28).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of restriction endonucleases for mapping the allele for beta s-globin

1 reference

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reference URL

https://api.crossref.org/works/10.1038%2F306701A0

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7 January 2021

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Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

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7 January 2021

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α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene

1 reference

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reference URL

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7 January 2021

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Absence of maternal contamination of chorionic villi used for fetal-gene analysis

1 reference

stated in

Crossref

reference URL

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7 January 2021

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Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

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reference URL

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7 January 2021

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Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

stated in

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reference URL

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7 January 2021

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Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

1 reference

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Crossref

reference URL

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retrieved

7 January 2021

based on heuristic

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Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F306701A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322

1 reference

stated in

Crossref

reference URL

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retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation and characterization of cDNA clones for human skeletal muscle α actin

1 reference

stated in

Crossref

reference URL

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retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/306701A0

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

Dimensions Publication ID

1010544637

0 references

PubMed publication ID

6689201

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6689201

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/6689201

 

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