(Q60641492)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348049%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2. (English)

1 reference

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14 September 2019

1

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14 September 2019

Ian W. Craig

5

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14 September 2019

author name string

N Tommerup

2

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14 September 2019

T Tønnesen

3

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14 September 2019

J Kreuder

4

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14 September 2019

N Horn

6

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14 September 2019

publication date

1 March 1992

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14 September 2019

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14 September 2019

volume

88

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14 September 2019

issue

6

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14 September 2019

page(s)

668-672

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https://scigraph.springernature.com/pub.10.1007/bf02265295

14 September 2019

exact match

0 references

cites work

X-linked genetic homologies between mouse and man.

1 reference

12 December 2020

Exclusion mapping of 12 X-linked disease loci and 10 DNA probes from the long arm of the X-chromosome

1 reference

12 December 2020

Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19

1 reference

12 December 2020

Localization of the X inactivation centre on the human X chromosome in Xq13.

1 reference

12 December 2020

Variability in clinical expression of Menkes syndrome

1 reference

12 December 2020

Duplication 5q(5q22----5q33): from an intrachromosomal insertion

1 reference

12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

12 December 2020

Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding

1 reference

12 December 2020

Parental origin of de novo chromosome rearrangements

1 reference

12 December 2020

[Specific fluorescence of R and G bands in human chromosomes]

1 reference

12 December 2020

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1 reference

12 December 2020

Menkes syndrome in a girl with X-autosome translocation

1 reference

12 December 2020

Linkage studies in Menkes' disease. The Xg blood group system and C-banding of the X chromosome.

1 reference

12 December 2020

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

1 reference

12 December 2020

Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.

1 reference

12 December 2020

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes

1 reference

12 December 2020

Prenatal and postnatal diagnosis of Menkes disease, an inherited disorder of copper metabolism

1 reference

12 December 2020

Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp

1 reference

12 December 2020

Localization of the gene encoding human erythroid-potentiating activity to chromosome region Xp11.1----Xp11.4.

1 reference

12 December 2020

Evidence that the Menkes locus maps on proximal Xp.

1 reference

12 December 2020

Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1

1 reference

12 December 2020

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

12 December 2020

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02265295

1 reference

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14 September 2019

1 reference