Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up
Experimental & Molecular Medicine
;
: 134-136, 1999.
Article
in English
| WPRIM
| ID: wpr-36358
ABSTRACT
We report the first de novo case of a heterochromatic duplication on the long arm of the chromosome 9, which then was pericentrically inverted at p11q13. This condition was detected prenatally and carry to term. We then performed the follow up for over 1 year. So far, there seems to be no phenotypical abnormalities.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Phenotype
/
Prenatal Diagnosis
/
Translocation, Genetic
/
Chromosomes, Human, Pair 9
/
Chromosomes, Human, Pair 11
/
Chromosome Aberrations
/
Chromosome Banding
/
In Situ Hybridization, Fluorescence
/
Gene Duplication
/
Chromosome Inversion
Type of study:
Diagnostic study
Limits:
Adult
/
Female
/
Humans
/
Pregnancy
Language:
English
Journal:
Experimental & Molecular Medicine
Year:
1999
Type:
Article
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