(Q41507349)

1 October 2017

title

Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses (English)

1 reference

1 October 2017

Yoshiura K

1

1 reference

1 October 2017

Inazawa J

2

1 reference

1 October 2017

Koyama K

3

1 reference

1 October 2017

Nakamura Y

4

1 reference

1 October 2017

Niikawa N

5

1 reference

1 October 2017

language of work or name

1 reference

1 January 1994

1 reference

Genes, Chromosomes and Cancer

1 October 2017

published in

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1 October 2017

volume

9

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1 October 2017

issue

1

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1 October 2017

page(s)

57-61

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Construction of mouse A9 clones containing a single human chromosome tagged with neomycin-resistance gene via microcell fusion

1 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Fine mapping and cloning of the breakpoint associated with Menkes syndrome in a female patient

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Isolation and mapping of 88 new RFLP markers on human chromosome 8

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46,XY or XX,del(8)(q23.3q24.13)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopic in situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Multiple exostoses in a patient with t(8;11)(q24.11;p15.5)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

The proximity of DNA sequences in interphase cell nuclei is correlated to genomic distance and permits ordering of cosmids spanning 250 kilobase pairs

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870090110

7 January 2021

Identifiers

DOI

10.1002/GCC.2870090110

1 reference

1 October 2017

1 reference