Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/1750-1172-1-26.pdf
Reference18 articles.
1. De Hert M, Steemans D, Theys P, Fryns JP, Peuskens J: Lujan-Fryns syndrome in the differential diagnosis of schizophrenia. Am J Med Genet. 1996, 67: 212-214. 10.1002/(SICI)1096-8628(19960409)67:2<212::AID-AJMG13>3.0.CO;2-M.
2. Wittine LM, Josephson KD, Williams MS: Aortic root dilation in apparent Lujan-Fryns syndrome. Am J Med Genet. 1999, 86: 405-409. 10.1002/(SICI)1096-8628(19991029)86:5<405::AID-AJMG2>3.0.CO;2-1.
3. Stathopulu E, Mackie Ogilvie C, Flinter FA: Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndrome. Am J Med Genet. 2003, 119A: 363-366. 10.1002/ajmg.a.10268.
4. Lujan JE, Carlin ME, Lubs HA: A form of X-linked mental retardation with marfanoid habitus. Am J Med Genet. 1984, 17: 311-322. 10.1002/ajmg.1320170124.
5. Fryns JP, Buttiens M: X-linked mental retardation with marfanoid habitus. Am J Med Genet. 1987, 28: 267-274. 10.1002/ajmg.1320280202.
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