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Heritable Heteromorphism of the N. 16 Chromosome Pair in Man*

Published online by Cambridge University Press:  01 August 2014

G. Guanti ,
C. Balacco-Gabrieli  and
E. Battaglia
G. Guanti*
Affiliation:
Institute of Genetics, University of Bari, Italy
C. Balacco-Gabrieli*
Affiliation:
Institute of Clinical Oculistics, University of Bari, Italy
E. Battaglia*
Affiliation:
Institute of Genetics, University of Bari, Italy
*
Istituto di Genetica, Via Amendola 165A, 70126 Bari, Italia
Clinica Oculistica, Policlinico, 70124 Bari, Italia
Istituto di Genetica, Via Amendola 165A, 70126 Bari, Italia

Summary

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A family is described with heteromorphism of N. 16 chromosome pair. The abnormal submetacentric chromosome was found in a total of 8 family members. Seven out of these carriers show a variable degree of myopia.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 18 , Issue 1 , January 1969 , pp. 77 - 85
Copyright
Copyright © The International Society for Twin Studies 1969

Footnotes

*

The study was made possible by support from the National Council of Researches (CNR).

References

Bray, P. F., Mukherjee, B. B. (1963). A chromosome anomaly in an infant with a degenerative disease of the central nervous system. J. Pediat., 62: 230.Google Scholar
Carr, D. H. (1963). Chromosomal abnormalities and their relation to disease. Canad. Med. Ass. J., 88: 456.Google ScholarPubMed
Court Brown, W. M., Jacobs, P., Brunton, M. (1965). Chromosome studies on randomly chosen men and women. Lancet, 2: 591.Google Scholar
Crawford, M. N., Punnett, H. H., Carpenter, G. G. (1967). Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage. Nature, 215: 1075.Google Scholar
De Morsier, G., Gauthier, G. (1963). La dysplasie olfacto-génitale. Path. Biol., 11: 1267.Google Scholar
Frederic, J., Lennes, G., Ronge-Collard, E., Mouchette, R., Hausman-Hagemeijer, A. (1967). Mise en évidence par analyse statistique d'une petite translocation chez un sujet atteint du syndrome de Stein-Leventhal. J. Genet. Hum., 16: 25.Google ScholarPubMed
German, J., Ehlers, K. H., Engle, M. A. (1966). Familial congenital heart disease. II. Chromosomal studies. Circulation, 34: 517.Google Scholar
Grimaud, R., Gilgenkrantz, M. S., Bemol, P. (1967). Anomalies morphologiques des chromosomes de la 16 paire et appareil auditif. Acta Otolaringol., 63: 44.Google Scholar
Hall, B. (1964). Mongolism in newborns. A clinical and cytogenetic study. Acta Pediat., Suppl. 54.Google Scholar
Hungerford, D. A. (1965). Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCL1 . Stain Technol., 40: 333.Google Scholar
Jacobs, P. A., Brunton, M., Court Brown, W. M. (1964). Cytogenetic studies in leucocytes on the general population: subjects of ages 65 years and more. Ann. Hum. Genet., 27: 353.Google Scholar
Jennings, A. A., Turner, B. (1961). Autosomal chromosome anomalies. Med. J. Austral., 2: 830.Google Scholar
Kelly, S., Almy, R. (1966). No. 16 Chromosome in Congenital Heart Disease. Personal Communication.Google Scholar
Kelly, S., Almy, R. (1966). Homology of No. 16 chromosome in congenital heart disease. Abstr. 5th. Conf. Mammal. Cytol. Somat. Cell Genet., 8: 38.Google Scholar
Lejeune, J. (1966). Personal Communication, (cf Frederic J., Lennès G., Rongé-Collard E., Mouchette R. and Hausman-Hagemeijer A., p. 39).Google Scholar
Makino, S. (1963). Session 1, Discussion. 2nd Int. Conf. Congen. Malform. New York, 74.Google Scholar
Makino, S. (1964). Chromosomal studies in normal human subjects and in 300 cases of congenital disorders. Cytologia, 29: 126.Google ScholarPubMed
Moores, E. C., Anders, J. M., Emanuel, R. (1966). Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease. Ann. Hum. Genet., 30: 77.Google Scholar
Nuzzo, F., Caviezel, F., de Carli, L. (1966). Y Chromosome and exclusion of paternity. Lancet, 2: 260.Google Scholar
Sasaki, M. S., Marino, S. (1963). Chromosomal aberrations in congenital cardiovascular disorders of man. Proc. Jap. Acad., 39: 394.Google Scholar
Starkman, M. N., Shaw, M. (1967). Atypical acrocentric chromosomes in Negro and Caucasian mongols. Amer. J. Hum. Genet., 19: 162.Google Scholar
Therkelsen, A. J., Lamm, L. U., Henningsen, K. (1967). Heritable morphological differences between the two chromosomes N. 16 in humans. Hereditas, 57: 149.Google Scholar
Tips, R. L., Smith, G. S., Meyer, D. L., Perkins, A. L. (1964). Familial mosaicism of a chromosome 16 abnormality associated with multiple congenital anomalies. Amer. J. Ment. Defic, 69: 330.Google ScholarPubMed