A newly recognized chondrodysplasia with multiple dislocations
- PMID: 15368507
- DOI: 10.1002/ajmg.a.30179
A newly recognized chondrodysplasia with multiple dislocations
Similar articles
-
The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profile.Genet Couns. 1993;4(2):157-64. Genet Couns. 1993. PMID: 8357567
-
Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance.J Med Genet. 2002 Sep;39(9):666-70. doi: 10.1136/jmg.39.9.666. J Med Genet. 2002. PMID: 12205110 Free PMC article. No abstract available.
-
Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.Am J Hum Genet. 2008 Jun;82(6):1368-74. doi: 10.1016/j.ajhg.2008.05.006. Am J Hum Genet. 2008. PMID: 18513679 Free PMC article.
-
Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type: report of a new patient and review of the literature.Am J Med Genet A. 2003 Oct 15;122A(3):252-6. doi: 10.1002/ajmg.a.20262. Am J Med Genet A. 2003. PMID: 12966527 Review.
-
Blomstrand chondrodysplasia: a lethal sclerosing skeletal dysplasia. Case report and review.Pediatr Radiol. 1999 Nov;29(11):842-5. doi: 10.1007/s002470050709. Pediatr Radiol. 1999. PMID: 10552065 Review.
Cited by
-
Epidemiology, etiology, and genetic aspects of reduction deficiencies of the lower limb.J Child Orthop. 2008 Oct;2(5):329-32. doi: 10.1007/s11832-008-0098-9. Epub 2008 Apr 9. J Child Orthop. 2008. PMID: 19308564 Free PMC article.
-
A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.J Community Genet. 2015 Jan;6(1):83-105. doi: 10.1007/s12687-014-0203-3. Epub 2014 Sep 27. J Community Genet. 2015. PMID: 25261319 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical