JNM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


The Journal of Nuclear Medicine Vol. 6 No. 10 740-746
© 1965 by Society of Nuclear Medicine
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dekaban, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dekaban, A.

Persisting Clone of Cells With an Abnormal Chromosome in a Woman Previously Irradiated

Anatole Dekaban, M.D.1

Bethesda, Maryland

ABSTRACT

Chromosome studies performed on the mother who gave birth to a dystrophic and malformed child showed two types of abnormality. The first abnormality consisted of a clone of cells characterized by frequent breaks in the same general region of long arms in the presumed chromosome No. 9. Since this was observed in the repeated blood cultures but not in the skin culture, the clone is probably confined to the blood forming tissue. The second abnormality consisted of a moderately increased rate of chromosome-type aberrations occurring at random in all chromosomes. This woman received 1550 rads to the skin for treatment of eczematous dermatitis during the preceding 16 years, resulting in an estimated dose of 242 rads to portions of the bone marrow and lymph nodes. The type of random chromosome abnormality observed in her blood cultures has been reported previously to be associated with exposure to radiation. The aberrant cell clone may also have been induced by the same etiological factor.

FOOTNOTES

1 Section on Child Neurology, SN, NINDB, National Institutes of Health, Bethesda, Maryland.




This article has been cited by other articles:


Home page
Hum Mol GenetHome page
K. Debacker and R.F. Kooy
Fragile sites and human disease
Hum. Mol. Genet., October 15, 2007; 16(R2): R150 - R158.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Y. Y. Hsu and Y.-H. Wang
Human Fragile Site FRA16B DNA Excludes Nucleosomes in the Presence of Distamycin
J. Biol. Chem., May 3, 2002; 277(19): 17315 - 17319.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
R. E. Magenis, F. Hecht, and E. W. Lovrien
Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man
Science, October 2, 1970; 170(3953): 85 - 87.
[Abstract] [PDF]


Home page
ScienceHome page
S. Irwin and J. Egozcue
Chromosomal Abnormalities in Leukocytes from LSD-25 Users
Science, July 21, 1967; 157(3786): 313 - 314.
[Abstract] [PDF]


Home page
ScienceHome page
M. M. Cohen, M. J. Marinello, and N. Back
Chromosomal Damage in Human Leukocytes Induced by Lysergic Acid Diethylamide
Science, March 17, 1967; 155(3768): 1417 - 1419.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY THE JOURNAL OF NUCLEAR MEDICINE
Copyright © 1965 by the Society of Nuclear Medicine.