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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2006-3-10
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pubmed:abstractText |
Deletion of 15q21q22 is a rare chromosomal anomaly. To date, there have been nine reports describing ten individuals with different segmental losses involving 15q21 and 15q22. Many of these individuals have common features of growth retardation, hypotonia and moderate to severe mental retardation. Congenital heart disease has been described in three individuals with interstitial deletion involving this region of chromosome 15.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-10319204,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-11044437,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-11136687,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-11178108,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-11839628,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-12684692,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-12915473,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-16179230,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-2158525,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-2246774,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-2368808,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-3198122,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-3430549,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16472378-6979302
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
1471-2350
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:16472378-Aortic Coarctation,
pubmed-meshheading:16472378-Child, Preschool,
pubmed-meshheading:16472378-Chromosome Deletion,
pubmed-meshheading:16472378-Chromosomes, Human, Pair 15,
pubmed-meshheading:16472378-Cytogenetic Analysis,
pubmed-meshheading:16472378-Developmental Disabilities,
pubmed-meshheading:16472378-Facies,
pubmed-meshheading:16472378-Humans,
pubmed-meshheading:16472378-In Situ Hybridization, Fluorescence,
pubmed-meshheading:16472378-Male,
pubmed-meshheading:16472378-Nucleic Acid Hybridization
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pubmed:year |
2006
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pubmed:articleTitle |
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2).
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pubmed:affiliation |
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA. seemal@bcm.tmc.edu
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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