Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46,XY or XX,del(8)(q23.3q24.13)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00289486.pdf
Reference15 articles.
1. Beighle C, Karp LE, Hanson JW, Hall JG, Hoehn H (1977) Small structural changes of chromosome 8. Hum Genet 38:113?121
2. Bühler EM, Bühler UK, Stalder GR, Jani L, Jurik LP (1980) Chromosome deletion and multiple cartilaginous exostoses. Eur J Pediatr 133:163?166
3. Dallapiccola B, Santoro L, Trabace S, Ramenghi M, Mastroiacovo P, Gandini E (1977) Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8)(q13;q213). Hum Genet 38:125?130
4. Frontali M, Ramenghi M, Trabace S, Dallapiccola B (1982) Microcytogenetics and Langer-Giedion syndrome. J Med Genet 19:390?391
5. Fryns JP, Logghe N, Eygen MV, Berghe VD (1979) Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21). Hum Genet 48:127?130
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