Terminal long-arm deletion of chromosome 1 in a male infant
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00286898.pdf
Reference10 articles.
1. Andrle, M., Erlach, A., Mayr, W. R., Rett, A.: Terminal deletion of (1)(q42) and its phenotypical manifestations. Hum. Genet. 41, 115?120 (1978)
2. Boué, J., Boué, A., Lazar, P.: Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions. Teratology 12, 11?26 (1975)
3. Garver, K. L., Ciocco, A. M., Turack, N. A.: Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1. Clin. Genet. 10, 319?324 (1976)
4. Hamerton, J. L.: Human cytogenetics. Vol. 1, pp. 265. New York: Academic Press 1971
5. Kessel, E., Pfeiffer, R. A., Blanke, W., Schwarz, J.: Terminal deletion of the long arm of chromosome 1 in a malformed newborn. Hum. Genet. 42, 333?337 (1978)
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