Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1978-4-17
|
| pubmed:abstractText |
Two patients with retinoblastoma and an interstitial deletion of the long arm of chromosome 13 were studied using G-banded metaphase and prophase chromosomes. One patient showed several congenital defects, developmental retardation, and deletion of bands q14 and q21. The second patient showed mild developmental delay, a few minor congenital defects, and a loss of approximately half of band q14. On the basis of this study and nine others from the literature, it is now possible to tentatively assign a predisposition to retinoblastoma to deletion of a specific small region of chromosome 13.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0002-922X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
132
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
161-3
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:626181-Abnormalities, Multiple,
pubmed-meshheading:626181-Chromosome Deletion,
pubmed-meshheading:626181-Chromosomes, Human, 13-15,
pubmed-meshheading:626181-Eye Neoplasms,
pubmed-meshheading:626181-Female,
pubmed-meshheading:626181-Humans,
pubmed-meshheading:626181-Infant,
pubmed-meshheading:626181-Karyotyping,
pubmed-meshheading:626181-Male,
pubmed-meshheading:626181-Retinoblastoma
|
| pubmed:year |
1978
|
| pubmed:articleTitle |
Retinoblastoma and subband deletion of chromosome 13.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|