Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb01025.x/fullpdf
Reference10 articles.
1. Small structural changes of chromosome 8;Beighle;Hum. Genet.,1977
2. Chromosome deletion and multiple cartilaginous exostoses;Bühler;Europ. J. Pediat.,1980
3. Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213);Dallapiccola;Hum. Genet.,1977
4. Interstitial deletion of the long arm of chromosome 8;Fryns;Hum. J. Genet.,1979
5. Deficit i psichico e malformazio ereditarie;Gedda;Acta med. auxol.,1971
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1. Long-term follow-up of four patients with langer-giedion syndrome: Clinical course and complications;American Journal of Medical Genetics Part A;2013-08-02
2. Clinical and molecular characterization of a patient with Langer-Giedion syndrome and mosaic del(8)(q22.3q24.13);American Journal of Medical Genetics Part A;2008-12-15
3. Langer-Giedion syndrome with del 8 (q24.13-q24.22);Clinical Genetics;2008-06-28
4. Tricho-rhino-phalangeal syndrome without exostoses, with an interstitial deletion of 8q23;Clinical Genetics;2008-04-23
5. A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome;Clinical Genetics;2008-04-23
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