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H. Evans (1973)
Molecular architecture of human chromosomes.British medical bulletin, 29 3
Evans Evans, Buckland Buckland, Pardue Pardue (1974)
Location of genes coding for 18S and 28S ribosomal RNA in the human genomeChromosoma, 48
A. Craig-Holmes, F. Moore, M. Shaw (1973)
Polymorphism of human C-band heterochromatin. I. Frequency of variants.American journal of human genetics, 25 2
A. Craig-Holmes, F. Moore, M. Shaw (1975)
Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.American journal of human genetics, 27 2
(1971)
Quinacrine fluorescence of variant and abnormal Y chromosomes
David Hungerford (1965)
Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl.Stain technology, 40 6
J. Nielsen (1975)
Chromosome examination of newborn children: purpose and ethical aspects.Humangenetik, 26 3
Caspersson Caspersson, Lomakka Lomakka, Zech Zech (1971)
The 24 fluorescing patterns of human chromosomes—distinguishing patterns and variabilityHereditas (Lund), 67
T. Caspersson, G. Lomakka, L. Zech (2009)
The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.Hereditas, 67 1
P. Jacobs, M. Melville, S. Ratcliffe, A. Keay, J. Syme (1974)
A cytogenetic survey of 11,680 newborn infantsAnnals of Human Genetics, 37
(1971)
Standardization in Human Cytogenetice
J. Robinson, K. Buckton, G. Spowart, M. Newton, P. Jacobs, H. Evans, R. Hill (1976)
The segregation of human chromosome polymorphismsAnnals of Human Genetics, 40
A. Henderson, D. Warburton, K. Atwood (1973)
Ribosomal DNA Connectives between Human Acrocentric ChromosomesNature, 245
J. Gosden, A. Mitchell, R. Buckland, R. Clayton, H. Evans (1975)
The location of four human satellite DNAs on human chromosomes.Experimental cell research, 92 1
SUMMARY The segregation of the Q‐band polymorphisms in 32 families have been studied. From 90 matings in these families, there were a total of 208 offspring. In one of these offspring it could be shown that there had been a change of a fluorescent polymorphism, resulting in the loss of fluorescent intensity in the satellite of a chromosome 21. The origin of such a ‘mutation’ and a consideration of mutation rates is discussed.
Annals of Human Genetics – Wiley
Published: Jan 1, 1978
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