A Chromosome 13q+in a patient with characteristics of the trisomy 13 syndrome

Author:

Hoehn H.,Wolf U.,Schumacher H.,Wehinger H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Arrighi, F., Hsu, T. C.: Localization of heterochromatin in human chromosomes. Cytogenetics 10, 81?86 (1971).

2. Betke, K., Marti, H. R., Schlicht, I.: Estimation of small percentages of foetal hemoglobin. Nature (Lond.) 184, 1877 (1959).

3. Bloom, G. E., Gerald, P. S.: Localisation of genes on chromosome 13: analysis of two kindreds. Amer. J. hum. Genet. 20, 495?511 (1968).

4. Bowen, P., Lee, C. S. N., Shea, D. R., Armstrong, H. B.: Polydactyly and other minor stigmata associated with 46 XX/47 XX D+mosaicism. Canad. med. Ass. J. 102, 49?51 (1970).

5. Green, J. R., Krovetz, L. H., Taylor, W. J.: Two generations of 13?15 chromosomal mosaicism: Possible evidence for a genetic defect in the control of chromosome replication. Cytogenetics 7, 286?297 (1968).

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