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PUBMED FOR HANDHELDS
Journal Abstract Search
249 related items for PubMed ID: 18841068
1. Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic or Hall type: report of a case with normal face and literature review. Sulko J, Kozlowski K. J Pediatr Orthop B; 2008 Nov; 17(6):323-7. PubMed ID: 18841068 [Abstract] [Full Text] [Related]
2. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL): a Brazilian case. Pina-Neto JM, Defino HL, Guedes ML, Jorge SM. Am J Med Genet; 1996 Jan 11; 61(2):131-3. PubMed ID: 8669438 [Abstract] [Full Text] [Related]
3. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL). Tsirikos AI, Mason DE, Scott CI, Chang WN. Am J Med Genet A; 2003 Jun 15; 119A(3):386-90. PubMed ID: 12784311 [Abstract] [Full Text] [Related]
11. A hypoplastic atlas and long odontoid process in a girl manifesting phenotypic features resembling spondyloepimetaphyseal dysplasia joint laxity syndrome. Al Kaissi A, Chehida FB, Ghachem MB, Klaushofer K, Grill F. Skeletal Radiol; 2008 May 15; 37(5):469-73. PubMed ID: 18256824 [Abstract] [Full Text] [Related]
12. Spondyloepimetaphyseal dysplasia (Hall type) with laryngeal stenosis: a new diagnostic feature? Holder-Espinasse M, Fayoux P, Morillon S, Fourier C, Dieux-Coeslier A, Manouvrier-Hanu S, Le Merrer M, Hall CM. Clin Dysmorphol; 2004 Jul 15; 13(3):133-135. PubMed ID: 15194947 [Abstract] [Full Text] [Related]
13. Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders. Colombi M, Dordoni C, Chiarelli N, Ritelli M. Am J Med Genet C Semin Med Genet; 2015 Mar 15; 169C(1):6-22. PubMed ID: 25821090 [Abstract] [Full Text] [Related]