(Q36804678)

16 August 2017

title

Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region (English)

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16 August 2017

B de Gouyon

1

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16 August 2017

A Chatterjee

2

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16 August 2017

A Monaco

3

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16 August 2017

N Quaderi

4

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16 August 2017

S D Brown

5

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16 August 2017

G E Herman

6

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16 August 2017

publication date

1 August 1996

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16 August 2017

number of pages

5

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inferred from page(s)

published in

Mammalian Genome

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16 August 2017

volume

7

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16 August 2017

issue

8

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16 August 2017

page(s)

575-579

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https://scigraph.springernature.com/pub.10.1007/s003359900172

16 August 2017

exact match

0 references

cites work

Complete sequence of a 38.4-kb human cosmid insert containing the polymorphic marker DXS455 from Xq28.

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https://api.crossref.org/works/10.1007%2FS003359900172

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

21 January 2018

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Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeast

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Genetic and physical mapping of the biglycan gene on the mouse X chromosome

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

A 2.3-Mb yeast artificial chromosome contig spanning from Gabra3 to G6pd on the mouse X chromosome

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Cloning and characterization of the cDNA for the murine iduronate sulfatase gene

21 January 2018

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Centronuclear myopathy: clinical, morphological and genetic characters. A review of 288 cases

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900172

Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children.

21 January 2018

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The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction

21 January 2018

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Construction of a large-insert yeast artificial chromosome library of the mouse genome

21 January 2018

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Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

21 January 2018

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X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28

21 January 2018

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Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources

21 January 2018

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YAC contig organization and CpG island analysis in Xq28.

21 January 2018

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A YAC clone map spanning 7.5 megabases of human chromosome band Xq28.

21 January 2018

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Genomic analysis using a yeast artificial chromosome library with mouse DNA inserts

21 January 2018

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A linkage study of a large pedigree with X linked centronuclear myopathy

21 January 2018

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X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci

21 January 2018

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130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus

21 January 2018

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The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies

21 January 2018

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

21 January 2018

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Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouse

21 January 2018

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Identification of tissue-specific expressed sequences in human band Xq28 with complex pig cDNA probes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes

21 January 2018

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

21 January 2018

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Report of the Committee on the Genetic Constitution of Chromosome 1

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Genetic mapping of the mouse X chromosome in the region homologous to human Xq27–Xq28

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

X-linked myotubular myopathy: clinical observations in ten additional cases

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900172

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900172

Genetic linkage heterogeneity in myotubular myopathy

21 January 2018

1 reference

12 December 2020

Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28

1 reference

12 December 2020

A genetic map of the mouse suitable for typing intraspecific crosses

1 reference

12 December 2020

Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region.

1 reference

12 December 2020

Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

1 reference

12 December 2020

1 reference

12 December 2020

Identifiers

DOI

10.1007/S003359900172

1 reference

16 August 2017

1 reference