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11. A newly recognized syndrome of connective tissue dysplasia in siblings (previously described as a variant of Morquio disease). Spellacy E; Gibbs DA; Watts RW Q J Med; 1981; 50(200):377-415. PubMed ID: 6805033 [TBL] [Abstract][Full Text] [Related]
12. [Study of congenital osteodystrophies. Considerations on 4 cases of Rathbun's hypophosphatasia and 7 unusual cases of rachitic osteodystrophy]. Tirnoveanu G; Georgescu MI; Mitescu G Rev Med Chir Soc Med Nat Iasi; 1972; 16(3):667-72. PubMed ID: 5080559 [No Abstract] [Full Text] [Related]
13. Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity. Bonaventure J; Stanescu R; Stanescu V; Allain JC; Muriel MP; Ginisty D; Maroteaux P Am J Med Genet; 1992 Dec; 44(6):738-53. PubMed ID: 1481841 [TBL] [Abstract][Full Text] [Related]
14. A syndrome of systemic hyalinosis, short-limb dwarfism and possible thymic dysplasia. Alfi OS; Heuser ET; Landing BH; Robinson RE; Nadler S; Donnell GN Birth Defects Orig Artic Ser; 1975; 11(5):57-62. PubMed ID: 56200 [No Abstract] [Full Text] [Related]
15. Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome. Evans BR; Mosig RA; Lobl M; Martignetti CR; Camacho C; Grum-Tokars V; Glucksman MJ; Martignetti JA Am J Hum Genet; 2012 Sep; 91(3):572-6. PubMed ID: 22922033 [TBL] [Abstract][Full Text] [Related]
16. [Metacarpophalangeal pattern as well as length and proportions of the bones of the extremities in an infant with Robinow's syndrome II]. Oliván Gonzalvo G; Sarriá Chueca A; Ventura Faci P; Pérez González JM; Bueno Sánchez M An Esp Pediatr; 1990 Jul; 33(1):82-4. PubMed ID: 2252297 [No Abstract] [Full Text] [Related]
17. [Current status of the physiology and new trends in the pathology of connective tissue. IV. Nosology and nosography of primary diffuse diseases of connective tissue]. Lenzi L; Silva E Chir Organi Mov; 1968; 56(3):196-236. PubMed ID: 4245323 [No Abstract] [Full Text] [Related]
18. A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesis. Meigel WN; Müller PK; Pontz BF; Sörensen N; Spranger J Klin Wochenschr; 1974 Oct; 52(19):906-12. PubMed ID: 4457717 [No Abstract] [Full Text] [Related]
19. [Hereditary bone dystrophy. Pyknodysostosis]. Sada Moreno E; Martinez Lage JL; Vazquez Ajuria F; Jimenez Burkhardt A Rev Esp Estomatol; 1980; 28(6):331-6. PubMed ID: 6798645 [No Abstract] [Full Text] [Related]