Author:
Fryns J. P.,De Waele P.,Van Den Berghe H.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference7 articles.
1. Fryns, J. P., Van Bosstraeten, B., Malbrain, H., Van den Berghe, H.: Interstitial deletion of the long arm of chromosome 2 in a poly-malformed newborn?karyotype: 46,XX,del(2) (q21q24). Hum. Genet. 39, 233?238 (1977)
2. Fryns, J. P., De Boeck, K., Jaeken, J., Van den Berghe, H.: Malformative syndrome associated with a ring chromosome 10 and a translocated 10q/1q chromosome. Hum. Genet. 43, 239?244 (1978)
3. German, J., Chaganti, R. J. K.: Mapping human autosomes, assignment of the MN locus to a specific in the long arm of chromosome no. 2. Science 182, 1261?1262 (1973)
4. Sills, J. A., Buckton, K. E., Raeburn, J. A.: Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q. J. Med. Genet. 13, 507?510 (1976)
5. Sutherland, G. R., Carter, R. F.: 46,XX/46,XX,r(p25q37) mosaicism: clinical and cytogenetic studies. Ann. Genet. (Paris) 21, 164?167 (1978)
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