These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
193 related articles for article (PubMed ID: 3001313)
1. Collagen genes and proteins in osteogenesis imperfecta. Pope FM; Nicholls AC; McPheat J; Talmud P; Owen R J Med Genet; 1985 Dec; 22(6):466-78. PubMed ID: 3001313 [TBL] [Abstract][Full Text] [Related]
2. Exclusion of the alpha 1(II) cartilage collagen gene as the mutant locus in type IA osteogenesis imperfecta. Sykes B; Smith R; Vipond S; Paterson C; Cheah K; Solomon E J Med Genet; 1985 Jun; 22(3):187-91. PubMed ID: 2989526 [TBL] [Abstract][Full Text] [Related]
3. Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2. Sykes B; Ogilvie D; Wordsworth P; Wallis G; Mathew C; Beighton P; Nicholls A; Pope FM; Thompson E; Tsipouras P Am J Hum Genet; 1990 Feb; 46(2):293-307. PubMed ID: 1967900 [TBL] [Abstract][Full Text] [Related]
4. Frameshift mutation near the 3' end of the COL1A1 gene of type I collagen predicts an elongated Pro alpha 1(I) chain and results in osteogenesis imperfecta type I. Willing MC; Cohn DH; Byers PH J Clin Invest; 1990 Jan; 85(1):282-90. PubMed ID: 2295701 [TBL] [Abstract][Full Text] [Related]
5. Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a mutation in the COL1A2 gene of type I collagen. The mosaic parent exhibits phenotypic features of a mild form of the disease. Edwards MJ; Wenstrup RJ; Byers PH; Cohn DH Hum Mutat; 1992; 1(1):47-54. PubMed ID: 1301191 [TBL] [Abstract][Full Text] [Related]
6. Strategy for prenatal diagnosis of osteogenesis imperfecta by linkage analysis to the type I collagen loci COL1A1 and COL1A2. Benušienė E; Kučinskas V Med Sci Monit; 2000; 6(2):217-26. PubMed ID: 11208313 [TBL] [Abstract][Full Text] [Related]
7. [A new mutation in COL1A1 gene in a family with osteogenesis imperfecta]. Wang Z; Xu DL; Chen Z; Hu JY; Yang Z; Wang LT Zhonghua Yi Xue Za Zhi; 2006 Jan; 86(3):170-3. PubMed ID: 16638323 [TBL] [Abstract][Full Text] [Related]
8. Osteogenesis imperfecta: comparison of molecular defects with bone histological changes. Sztrolovics R; Glorieux FH; Travers R; van der Rest M; Roughley PJ Bone; 1994; 15(3):321-8. PubMed ID: 7520724 [TBL] [Abstract][Full Text] [Related]
9. An osteopenic nonfracture syndrome with features of mild osteogenesis imperfecta associated with the substitution of a cysteine for glycine at triple helix position 43 in the pro alpha 1(I) chain of type I collagen. Shapiro JR; Stover ML; Burn VE; McKinstry MB; Burshell AL; Chipman SD; Rowe DW J Clin Invest; 1992 Feb; 89(2):567-73. PubMed ID: 1737847 [TBL] [Abstract][Full Text] [Related]
10. A cysteine for glycine substitution at position 1017 in an alpha 1(I) chain of type I collagen in a patient with mild dominantly inherited osteogenesis imperfecta. Labhard ME; Wirtz MK; Pope FM; Nicholls AC; Hollister DW Mol Biol Med; 1988 Dec; 5(3):197-207. PubMed ID: 3244312 [TBL] [Abstract][Full Text] [Related]
11. Segregation analysis of dominant osteogenesis imperfecta in Italy. Mottes M; Cugola L; Cappello N; Pignatti PF J Med Genet; 1990 Jun; 27(6):367-70. PubMed ID: 1972760 [TBL] [Abstract][Full Text] [Related]
12. Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe. Tsipouras P; Schwartz RC; Goldberg JD; Berkowitz RL; Ramirez F J Med Genet; 1987 Jul; 24(7):406-9. PubMed ID: 2886666 [TBL] [Abstract][Full Text] [Related]
13. Disrupted growth plates and progressive deformities in osteogenesis imperfecta as a result of the substitution of glycine 585 by valine in the alpha 2 (I) chain of type I collagen. Cole WG; Chan D; Chow CW; Rogers JG; Bateman JF J Med Genet; 1996 Nov; 33(11):968-71. PubMed ID: 8950681 [TBL] [Abstract][Full Text] [Related]
15. Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfecta. Tsipouras P; Børresen AL; Dickson LA; Berg K; Prockop DJ; Ramirez F Am J Hum Genet; 1984 Nov; 36(6):1172-9. PubMed ID: 6097110 [TBL] [Abstract][Full Text] [Related]
16. Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfecta. Williams EM; Nicholls AC; Daw SC; Mitchell N; Levin LS; Green B; MacKenzie J; Evans DR; Chudleigh PA; Pope FM Clin Genet; 1989 Mar; 35(3):181-90. PubMed ID: 2650933 [TBL] [Abstract][Full Text] [Related]
17. A single amino acid deletion in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type III. Molyneux K; Starman BJ; Byers PH; Dalgleish R Hum Genet; 1993 Feb; 90(6):621-8. PubMed ID: 8444468 [TBL] [Abstract][Full Text] [Related]
18. Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Chipman SD; Sweet HO; McBride DJ; Davisson MT; Marks SC; Shuldiner AR; Wenstrup RJ; Rowe DW; Shapiro JR Proc Natl Acad Sci U S A; 1993 Mar; 90(5):1701-5. PubMed ID: 8446583 [TBL] [Abstract][Full Text] [Related]
19. Clinical variability of osteogenesis imperfecta linked to COL1A2 and associated with a structural defect in the type I collagen molecule. Superti-Furga A; Pistone F; Romano C; Steinmann B J Med Genet; 1989 Jun; 26(6):358-62. PubMed ID: 2567784 [TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta type I-IV. Pollitt R; McMahon R; Nunn J; Bamford R; Afifi A; Bishop N; Dalton A Hum Mutat; 2006 Jul; 27(7):716. PubMed ID: 16786509 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]