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PMID: 3463440 Published · ppublish English Case Reports Journal Article

Structure, origin and effects of a supernumerary marker chromosome 15.

Clinical genetics ·Vol. 30 ·No. 1 ·1986-07-00 ·Pages 63-71

Schmid M, Schindler D, Haaf T

Abstract

A de novo supernumerary small marker chromosome 15 was observed in a female infant with mental and statomotoric retardation as well as minor facial dysmorphia. The marker chromosome was analyzed by ten different staining techniques and 5-azacytidine treatment of lymphocyte cultures. It is shown that the supernumerary chromosome was derived by a non-sister chromatid exchange between the two homologous maternal chromosomes 15. The cytogenetical properties of the marker chromosome, the different activity of its two nucleolus organizer regions and the somatic pairing configurations revealed by 5-azacyidine are reported.

MeSH Terms
Child, Preschool Chromosome Banding Chromosomes, Human, Pair 15 Face/abnormalities Female Genetic Markers Growth Disorders/genetics Humans Intellectual Disability/genetics Trisomy
Chemicals
Genetic Markers
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schmid M
Schindler D
Haaf T
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1986-07-00
Pages
63-71
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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