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27. [Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)]. Baujat G; Lebre AS; Cormier-Daire V; Le Merrer M Arch Pediatr; 2008 Jun; 15(5):789-91. PubMed ID: 18582751 [No Abstract] [Full Text] [Related]
28. A pedigree of osteogenesis imperfecta. Ray AK J Genet Hum; 1969 May; 17(1):69-74. PubMed ID: 5808542 [No Abstract] [Full Text] [Related]
29. Musculo-skeletal problems associated with pregnancy in women with osteogenesis imperfecta. McAllion SJ; Paterson CR J Obstet Gynaecol; 2002 Mar; 22(2):169-72. PubMed ID: 12521699 [TBL] [Abstract][Full Text] [Related]
30. Osteogenesis imperfecta: update and perspective. Byers PH; Bonadio JF; Steinmann B Am J Med Genet; 1984 Feb; 17(2):429-35. PubMed ID: 6702896 [No Abstract] [Full Text] [Related]
31. Two questions about osteogenesis imperfecta. Plotkin H J Pediatr Orthop; 2006; 26(1):148-9. PubMed ID: 16439922 [No Abstract] [Full Text] [Related]
32. A novel G1006A substitution in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type III. Lu J; Costa T; Cole WG Hum Mutat; 1995; 5(2):175-8. PubMed ID: 7749416 [No Abstract] [Full Text] [Related]
34. Scanning electron microscopy of teeth in dominant osteogenesis imperfecta: support for genetic heterogeneity. Levin LS; Brady JM; Melnick M Am J Med Genet; 1980; 5(2):189-99. PubMed ID: 7395911 [TBL] [Abstract][Full Text] [Related]
35. Clinical and genetic aspects in autosomal dominant inherited osteogenesis imperfecta type I. Garretsen TJ; Cremers CW Ann N Y Acad Sci; 1991; 630():240-8. PubMed ID: 1952595 [TBL] [Abstract][Full Text] [Related]
36. Osteogenesis imperfecta: the molecular basis of clinical heterogeneity. Byers PH; Bonadio JF; Cohn DH; Starman BJ; Wenstrup RJ; Willing MC Ann N Y Acad Sci; 1988; 543():117-28. PubMed ID: 3063158 [No Abstract] [Full Text] [Related]
38. A new culprit in osteogenesis imperfecta. Germain-Lee EL J Bone Miner Res; 2011 Dec; 26(12):2795-7. PubMed ID: 22105742 [No Abstract] [Full Text] [Related]
39. Osteogenesis imperfecta nosology and genetics. Sillence DO Ann N Y Acad Sci; 1988; 543():1-15. PubMed ID: 3063156 [No Abstract] [Full Text] [Related]
40. Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta. Thompson EM; Young ID; Hall CM; Pembrey ME Clin Genet; 1989 Dec; 36(6):464. PubMed ID: 2591074 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]