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2. Classic X-linked spondyloepiphyseal dysplasia tarda in a woman with normal karyotype. Monteiro de Pina Neto J; Bonfim MD; Ferrari I Prog Clin Biol Res; 1982; 104():127-32. PubMed ID: 6819575 [TBL] [Abstract][Full Text] [Related]
4. [Morquio's syndrome without abnormal excretion of mucopolysaccharides]. Velázquez M; Yáñez E; Zavala C; Ocaranza J; Pitol A; Lisker R Rev Invest Clin; 1970; 22(4):407-14. PubMed ID: 4258103 [No Abstract] [Full Text] [Related]
5. Two first cousins with spondyloepiphyseal dysplasia tarda (X linked recessive form), one also with poikiloderma atrophicans vasculare progressing to lymphocytic lymphoma. Branford WA; Beveridge GW; Wynne-Davies R J Med Genet; 1982 Jun; 19(3):210-3. PubMed ID: 6809944 [TBL] [Abstract][Full Text] [Related]
6. [Study on the urinary glycosaminoglycan of spondyloepiphyseal dysplasia congenita (author's transl)]. Masuda H; Shichijo S; Takeuchi M Rinsho Byori; 1976; 24(1):65-7. PubMed ID: 130508 [No Abstract] [Full Text] [Related]
9. [A study on the urinary acid mucopolysaccharide of the hereditary mucopolysaccharidosis IV (Morquio syndrome) (author's transl)]. Masuda H; Shichijo S; Imai H; Takeuchi M Rinsho Byori; 1975 Aug; 23(8):649-52. PubMed ID: 127864 [No Abstract] [Full Text] [Related]
10. Glycosaminoglycan from the urine of spondyloepiphyseal dysplasia congenita. Masuda H; Shichijo S; Takeuchi M Clin Chim Acta; 1975 Nov; 65(1):149-51. PubMed ID: 127676 [No Abstract] [Full Text] [Related]
11. Morquio-B disease, spondyloepiphyseal dysplasia associated with acid beta-galactosidase deficiency. Report of three cases in one family. van Gemund JJ; Giesberts MA; Eerdmans RF; Blom W; Kleijer WJ Hum Genet; 1983; 64(1):50-4. PubMed ID: 6409799 [TBL] [Abstract][Full Text] [Related]
12. X-linked spondyloepiphyseal dysplasia tarda: molecular cause of a heritable platyspondyly. Fiedler J; Frances AM; Le Merrer M; Richter M; Brenner RE Spine (Phila Pa 1976); 2003 Nov; 28(22):E478-82. PubMed ID: 14624098 [TBL] [Abstract][Full Text] [Related]
18. Recessively inherited, late onset spondylar dysplasia and peripheral corneal opacity with anomalies in urinary mucopolysaccharides: a possible error of chondroitin-6-sulfate synthesis. Toledo SP; Mourão PA; Lamego C; Alves CA; Dietrich CP; Assis LM; Mattar E Am J Med Genet; 1978; 2(4):385-95. PubMed ID: 122434 [TBL] [Abstract][Full Text] [Related]
19. Spondyloepiphyseal dysplasia tarda. A case report. Specht EE Clin Orthop Relat Res; 1968; 60():159-62. PubMed ID: 4236348 [No Abstract] [Full Text] [Related]