Inversion of ?fluorescent? segment in chromosome 3: A polymorphic trait

Author:

Soudek D.,Sroka Helena

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Buckton, K. E., O'Riordan, M. L., Jacobs, P. A., Robinson, J. A., Hill, R., Evans, H. J.: C- and Q-band polymorphism in the chromosomes of three human populations. Ann. Hum. Genet. 40, 99?112 (1976)

2. Lin, C. C., Gedeon, M. M., Griffith, P., Smink, W. K., Newton, D. R., Wilkie, L., Sewell, L. M.: Chromosomes analysis on 930 consecutive newborn children using Quinacrine fluorescent banding technique. Hum. Genet. 31, 315?328 (1976)

3. Mikelsaar, A.-V. N., Ilus, T., Kiwi, S.: Variant chromosome 3 (inv 3) in normal newborns and their parents, and in children with mental retardation. Hum. Genet. 41, 109?114 (1978)

4. Müller, H. J., Klinger, H. P., Glasser, M.: Chromosome polymorphism in a human newborn population. II. Cytogenet. Cell Genet 15, 239?255 (1975)

5. Pearson, P. L., Geraedts, J. P. M., van der Linden, A. G. J. M.: Human chromosome polymorphism. In: Modern Aspects of Cytogenetics: Constitutive Heterochromatin in Man (R. A. Pfeiffer, Ed.), pp. 203?213. Stuttgart-New York: Schattauer 1973

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