(Q45863462)

17 December 2017

title

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

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17 December 2017

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Camerino G

1

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17 December 2017

Mattei MG

2

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17 December 2017

Mattei JF

3

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17 December 2017

Jaye M

4

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17 December 2017

Mandel JL

5

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17 December 2017

publication date

1 December 1983

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17 December 2017

language of work or name

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17 December 2017

volume

306

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17 December 2017

issue

5944

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17 December 2017

page(s)

701-704

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17 December 2017

Nonspecific X-linked mental retardation--a review

cites work

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7 January 2021

High resolution banding and the locus of the Xq fragile site

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

7 January 2021

Brief report: linkage between G6PD and fragile-X syndrome

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Identifiers

DOI

10.1038/306701A0

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17 December 2017

Dimensions Publication ID

1010544637

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17 December 2017