Fragile site long arm chromosome 16
- 1 January 1979
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 48 (1) , 131-134
- https://doi.org/10.1007/bf00273287
Abstract
A fragile site at the long arms (q21) of chromosome 16 was found in two persons, each of whom became the parent of a child with a de novo structural chromosome abnormality—a balanced autosomal translocation and an autosomal deletion. The question of an increased risk of structural chromosome abnormalities in the offspring of persons with fragile site long arm 16 is discussed.Keywords
This publication has 10 references indexed in Scilit:
- Apparently balanced de novo translocations in patients with abnormal phenotypes: Report of 6 casesClinical Genetics, 1977
- The 11q- syndrome: Another case reportHuman Genetics, 1977
- [Interstitial deletion of the long arm of one 11 chromosome].1975
- An (11;21) Translocation in Four Generations with Chromosome 11 Abnormalities in the OffspringHuman Heredity, 1973
- Induced chromosomal aberrations: Biological and clinical significanceThe Journal of Pediatrics, 1972
- Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease.1971
- Apparently spontaneous chromosome damage in human leukocytes and the nature of chromatid gapsPublished by Springer Nature ,1971
- Analytical Review: Spontaneous Chromosomal Breakage and High Incidence of Leukemia in Inherited DiseaseBlood, 1971
- Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in ManScience, 1970
- THE INTERACTION OF VARIOUS DRUGS WITH HUMAN CHROMOSOMESCanadian Journal of Genetics and Cytology, 1969