Warfarin-induced brachytelephalangic chondrodysplasia punctata
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Link
http://www.nature.com/articles/jp201028.pdf
Reference9 articles.
1. Bennett CP, Berry AC, Maxwell DJ, Seller MJ . Chondrodysplasia punctata: another possible x-linked recessive case. Am J Med Genet 1992; 44: 795–799.
2. Shanske AL, Bernstein L, Herzog R . Chondrodysplasia punctata and maternal autoimmune disease: a new case and review of the literature. Pediatrics 2007; 102: 436–441.
3. Maroteaux P . Brachytelephalangic chondrodysplasia punctata: a possible-x-linked recessive form. Hum Genet 1989; 82: 167–170.
4. Bick D, Curry JR, McGill JR, Schorderet DF, Bux RC, Moore CM . Male infant with ichthyosis, Kallman syndrome, chondrodysplasia punctata and an Xp chromosome deletion. Am J Med Genet 1989; 33: 100–107.
5. Franco B, Meroni G, Parenti G, Levilliers J, Bernard L, Gebbia M et al. A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell 1995; 81: 15–25.
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