Mental retardation with pterygia, shortness and distinct facial appearance A new MCA/MR syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb00425.x/fullpdf
Reference9 articles.
1. Baraitser , M. 1982 A new camptodactyly syndrome. J. Med. Genet.
2. Cantu , J. M. H. Rivera Z. Nazará Q. Rojas A. Hernández D. García-Cruz 1980 Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder. Clin. Genet.
3. Chen , M. C. H. Chang R. P. Misra H. A. Peters N. S. Grijalva J. M. Opitz 1980 Multiple Pterygium Syndrome. Am. J. Med. Genet.
4. de Grouchy , J. C. Turleau 1982 Atlas des maladies chromosomiques
5. Hall , J. G. S. D. Reed G. Greene 1982 The distal arthrogryposes: Delineation of new entities - Review and Nosologic Discussion. Am. J. Med. Genet.
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Arthrogryposes (Multiple Congenital Contractures);Emery and Rimoin's Principles and Practice of Medical Genetics;2013
2. Haspeslagh syndrome without severe mental retardation and pterygia?;Clinical Genetics;2008-06-28
3. Mental retardation with pterygia, shortness and distinct facial appearance. Confirmation of a new MCA/MR syndrome;Clinical Genetics;2008-06-28
4. Clinical follow up of a girl with “mental retardation with pterygia, shortness and distinct facial appearance” (Haspeslagh syndrome);Clinical Genetics;2008-04-23
5. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003
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