|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
1985-7-15
|
|
pubmed:abstractText |
A somatic cell hybrid has been constructed and characterized using fibroblasts from a phenotypically normal woman who possesses an X chromosome with an interstitial deletion of the short arm. High-resolution banding indicates that the deleted segment is either Xp22.13-p11.4 or Xp22.11-p11.23. Southern blot hybridization to previously mapped DNA sequences confirms that the missing segment of the X chromosome is a deletion and not an interstitial translocation and supports the cytogenetic interpretation that the deletion extends proximal of Xp11.3 and therefore probably comprises Xp22.11-p11.23. Three further DNA sequences have been localized to the region of the deleted segment. The following order has been assigned to the seven probes used: Xpter-RC8-pXUT22-(OA1,C7,M2C)-L1.28-RD6 -Xcen.
|
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-1195397,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-219990,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-474618,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-5286856,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-561093,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6139558,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6300789,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6304647,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6324578,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6326147,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6461845,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6542494,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6547776,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6585184,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6684692,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6684693,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6729462,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-6959140,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2988331-7273954
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
May
|
|
pubmed:issn |
0002-9297
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
37
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
451-62
|
|
pubmed:dateRevised |
2010-11-18
|
|
pubmed:meshHeading |
pubmed-meshheading:2988331-Animals,
pubmed-meshheading:2988331-Chromosome Banding,
pubmed-meshheading:2988331-Chromosome Deletion,
pubmed-meshheading:2988331-Chromosome Mapping,
pubmed-meshheading:2988331-Cricetinae,
pubmed-meshheading:2988331-Cricetulus,
pubmed-meshheading:2988331-DNA,
pubmed-meshheading:2988331-DNA Restriction Enzymes,
pubmed-meshheading:2988331-Female,
pubmed-meshheading:2988331-Genetic Linkage,
pubmed-meshheading:2988331-Genetic Markers,
pubmed-meshheading:2988331-Humans,
pubmed-meshheading:2988331-Hybrid Cells,
pubmed-meshheading:2988331-Karyotyping,
pubmed-meshheading:2988331-Muscular Dystrophies,
pubmed-meshheading:2988331-Mutation,
pubmed-meshheading:2988331-X Chromosome
|
|
pubmed:year |
1985
|
|
pubmed:articleTitle |
Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
