PMID: 60278Mar 12, 1976Paper

Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique

Human Genetics
C C LinL M Sewell

Abstract

Chromosome analysing using quinacrine fluorescence was performed on 930 consecutive newborn infants. The total incidence of major chromosome aberrations including numerical changes of the sex chromosomes, and structural changes of autosomes, was 0.54%. Incidence of XYY (0.4%) and XXY (0.2%) were relatively higher as compared to other studies. About 0.75% of the newborn infants were found to have a variable bright fluorescent band located on the proximal area of the short arm (p11) rather than on the proximal long arm (q11) of chromosome No. 3. Attempts were also made to record the variable fluorescent regions on 7 autosomes and the Y chromosome.

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Citations

Dec 29, 1978·Human Genetics·A A McCrackenA M Clark
Nov 15, 2007·European Journal of Human Genetics : EJHG·Joan K MorrisPatricia Jacobs
Jan 1, 1980·Annals of Human Genetics·K E BucktonM Short
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Jun 1, 1980·Ophthalmology·B L Gallie
Dec 17, 2009·Developmental Disabilities Research Reviews·Richard BoadaNicole Tartaglia
Jan 1, 1981·Canadian Journal of Genetics and Cytology. Journal Canadien De Génétique Et De Cytologie·R S Verma, H Dosik
Nov 1, 1989·American Journal of Medical Genetics·C L BorovikE de C Costa
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Dec 7, 2007·The Journal of Clinical Endocrinology and Metabolism·David J Handelsman
Mar 1, 1979·Canadian Journal of Genetics and Cytology. Journal Canadien De Génétique Et De Cytologie·R S Verma, H Dosik
Sep 5, 2001·American Journal of Human Biology : the Official Journal of the Human Biology Council·Melanie BlacklessEllen Lee
Jul 1, 1981·Clinical Genetics·S BardhanK Davis
Mar 1, 1991·Jinrui idengaku zasshi. The Japanese journal of human genetics·T MaedaN Yabe

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