Clinical and cytogenetic studies of two infants with partial monosomy G
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00446618.pdf
Reference15 articles.
1. Caspersson, T., Zech, L., Johansson, C., Modest, E. J.: Identification of human chromosomes by DNA-binding fluorescent agents. Chromosoma (Berl.) 30, 215?227 (1970)
2. Crandall, B. F., Weber, F., Muller, H. M., Burwell, J. K.: Identification of 21r and 22r chromosomes by quinacrine fluorescence. Clin. Genet. 3, 264?270 (1972)
3. DeCicco, F., Steele, M. W., Pan, S., Park, S. C.: Monosomy of chromosome No. 22: A case report. J. Pediat. 83, 836?838 (1973)
4. Grippenberg, U., Elfving, J., Grippenberg, L.: A 45,XX,21-child: attempt at a cytological and clinical interpretation of the karyotype. J. med. Genet. 9, 110?115 (1972)
5. Halloran, K. H., Roy Breg, W., Mahoney, M. J.: 21 monosomy in a retarded female infant. J. med. Genet. 11, 386?389 (1974)
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