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69. Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait. Hall J Birth Defects Orig Artic Ser; 1974; 10(8):157-71. PubMed ID: 4218495 [No Abstract] [Full Text] [Related]
73. Spondylometaepiphyseal dysplasia in a mother and her child. Pettersson H; Nilsson KO Acta Radiol Diagn (Stockh); 1979; 20(1):241-51. PubMed ID: 110035 [TBL] [Abstract][Full Text] [Related]
74. Diagnostic evaluation, monitoring, and perioperative management of spinal cord compression in patients with Morquio syndrome. Charrow J; Alden TD; Breathnach CA; Frawley GP; Hendriksz CJ; Link B; Mackenzie WG; Manara R; Offiah AC; Solano ML; Theroux M Mol Genet Metab; 2015 Jan; 114(1):11-8. PubMed ID: 25496828 [TBL] [Abstract][Full Text] [Related]
75. [Clinical and radiographic evolution of Morquio-Ullrich disease]. Campailla E; Martinelli B Chir Organi Mov; 1969; 57(4):311-32. PubMed ID: 4978224 [No Abstract] [Full Text] [Related]
76. Molecular analysis of Turkish mucopolysaccharidosis IVA (Morquio A) patients: identification of novel mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene. Terzioglu M; Tokatli A; Coskun T; Emre S Hum Mutat; 2002 Dec; 20(6):477-8. PubMed ID: 12442278 [TBL] [Abstract][Full Text] [Related]
77. Mutation and polymorphism spectrum of the GALNS gene in mucopolysaccharidosis IVA (Morquio A). Tomatsu S; Montaño AM; Nishioka T; Gutierrez MA; Peña OM; Tranda Firescu GG; Lopez P; Yamaguchi S; Noguchi A; Orii T Hum Mutat; 2005 Dec; 26(6):500-12. PubMed ID: 16287098 [TBL] [Abstract][Full Text] [Related]
78. [Pseudo-achondroplastic dysplasia. Apropos of a case]. Pagniez B; Saint-Aubert P; Farriaux JP; Fontaine G Ann Pediatr (Paris); 1972 Dec; 19(12):897-903. PubMed ID: 4630443 [No Abstract] [Full Text] [Related]
79. A family study of spondyloepiphyseal dysplasia. Diamond LS J Bone Joint Surg Am; 1970 Dec; 52(8):1587-94. PubMed ID: 4991676 [No Abstract] [Full Text] [Related]
80. Mucopolysaccharidosis IVA: a novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine-6-sulfate sulfatase gene in an Afghanistan girl with classical Morquio disease. Fukuda S; Yamada N; Tomatsu S; Sukegawa K; Montaño AM; Hopwood JJ; Muller V; Orii T; Kondo N Jpn J Hum Genet; 1997 Jun; 42(2):317-22. PubMed ID: 9290256 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]