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PMID: 65472 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Journal of medical genetics ·Vol. 13 ·No. 6 ·1976-12-00 ·Pages 520-2

Neu RL, Ortega CC, Barg GA, Pinto W, Gardner LI, Howell WM, Denton TE

Abstract

A male infant with a partial trisomy 18 and a 46,XY, --21, t(18;21)(18qter replaced by 18q12::21 p13 replaced by 21 qter) chromosome complement is described. The translocation chromosome is of special interest because it includes the satellites of chromosome 21. This was shown by differential satellite staining with the ammoniacal-silver technique.

MeSH Terms
Ammonia Chromosome Aberrations Chromosomes, Human, 16-18 Chromosomes, Human, 21-22 and Y Humans Infant Male Silver Staining and Labeling Translocation, Genetic Trisomy
Chemicals
Silver Ammonia
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Neu R L
Ortega C C
Barg G A
Pinto W
Gardner L I
Howell W M
Denton T E
References (15)
15 references, click to expand
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Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
Published
1976-12-00
Pages
520-2
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1013484
Subset
IM
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