SMITH-LEMLI-OPITZ SYNDROME
Author:
Publisher
Wiley
Subject
Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1968.tb02954.x/fullpdf
Reference6 articles.
1. ‘A syndrome characterised by mental retardation, short stature craniofacial dysplasia and genital anomalies occurring in siblings.’;Blair;J. Pediat.,1966
2. ‘The syndrome of retardation with urogenital and skeletal anomalies in siblings.’;Dallaire;J. Pediat.,1966
3. ‘Smith-Lemli-Opitz syndrome.’;Fine;Amer. J. Dis. Child.,1968
4. ‘A case of the Smith-Lemli-Opitz syndrome of multiple congenital anomalies in association with dysplasia epiphysialis punctata.’;Gibson;Canad. med. Ass. J.,1965
5. ‘A familial syndrome of facial and skeletal anomalies associated with genital abnormality in the male and normal genitals in the female.’;Pinsky;J. Pediat.,1965
Cited by 3 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. Smith-Lemli-Opitz (RSH) syndrome bibliography: 1964-1993;American Journal of Medical Genetics;1994-05-01
2. Smith-Lemli-Opitz (RSH) syndrome bibliography;American Journal of Medical Genetics;1987-11
3. A new syndrome with features of the Smith-Lemli-Opitz and Meckel-Gruber syndromes in a sibship with cerebellar defects;American Journal of Medical Genetics;1987-02
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