Interstitial deletion for a region in the long arm of chromosome 16
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00286649.pdf
Reference17 articles.
1. Côté GB, Papadakou-Lagoyanni S, Kairis M (1980) Fryns syndrome without deletion 16q. Ann Genet (Paris)23: 171?172
2. Ferguson-Smith MA, Westerveld A (1982) Report of the committee on the genetic constitution of chromosomes 13 to 22. Cytogenet Cell Genet 32: 161?178
3. Fryns JP (1983) Personal communication
4. Fryns JP, Melchior S, Jaeken J, van den Berghe H (1977) Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16)(q21). Hum Genet 38: 343?346
5. Fryns JP, Bande-Knops J, van den Berghe H (1979) Partial monosomy of the long arm of chromosome 16: a distinct clinical entity? Hum Genet 46: 115?120
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