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.
129 related articles for article (PubMed ID: 6419953)
1. Lethal osteogenesis imperfecta congenita and a 300 base pair gene deletion for an alpha 1(I)-like collagen. Pope FM; Cheah KS; Nicholls AC; Price AB; Grosveld FG Br Med J (Clin Res Ed); 1984 Feb; 288(6415):431-4. PubMed ID: 6419953 [TBL] [Abstract][Full Text] [Related]
2. Lethal osteogenesis imperfecta and a collagen gene deletion. Length polymorphism provides an alternative explanation. Sykes BC; Ogilvie DJ; Wordsworth BP Hum Genet; 1985; 70(1):35-7. PubMed ID: 3997150 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Osteogenesis imperfecta phenotypes resulting from serine for glycine substitutions in the alpha2(I) collagen chain. Nuytinck L; Wettinck K; Freund M; Van Maldergem L; Fabry G; De Paepe A Eur J Hum Genet; 1997; 5(3):161-7. PubMed ID: 9272740 [TBL] [Abstract][Full Text] [Related]
5. Intron-mediated recombination may cause a deletion in an alpha 1 type I collagen chain in a lethal form of osteogenesis imperfecta. Barsh GS; Roush CL; Bonadio J; Byers PH; Gelinas RE Proc Natl Acad Sci U S A; 1985 May; 82(9):2870-4. PubMed ID: 3857621 [TBL] [Abstract][Full Text] [Related]
6. Ultrasonic and radiological features of osteogenesis imperfecta congenita: case report. Griffin ER; Webster JC; Almario VP Mil Med; 1983 Feb; 148(2):157-8. PubMed ID: 6405317 [No Abstract] [Full Text] [Related]
8. Radiological "metamorphosis" in a patient with severe congenital osteogenesis imperfecta. Pendola F; Borrone C; Filocamo M; Lituania M; Steinmann B; Superti-Furga A Eur J Pediatr; 1990 Mar; 149(6):403-5. PubMed ID: 2332008 [TBL] [Abstract][Full Text] [Related]
9. Osteogenesis imperfecta congenita. Five cases and review of the literature. Choi BS; Kim PK; Coe CJ; Chin DS Yonsei Med J; 1970; 11(1):45-53. PubMed ID: 5516843 [No Abstract] [Full Text] [Related]
10. The prenatal diagnosis of osteogenesis imperfecta congenita. Heller RH; Winn KJ; Heller RM Am J Obstet Gynecol; 1975 Feb; 121(4):572-3. PubMed ID: 1146889 [No Abstract] [Full Text] [Related]
11. Prenatal diagnosis of osteogenesis imperfecta congenita by means of fetography. Ogita S; Kamei T; Matsumoto M; Shimamoto T; Shimura K Eur J Pediatr; 1976 Oct; 123(3):179-86. PubMed ID: 976283 [TBL] [Abstract][Full Text] [Related]
12. Lethal perinatal osteogenesis imperfecta due to a type I collagen alpha 2(I) Gly to Arg substitution detected by chemical cleavage of an mRNA:cDNA sequence mismatch. Bateman JF; Moeller I; Hannagan M; Chan D; Cole WG Hum Mutat; 1992; 1(1):55-62. PubMed ID: 1284475 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of lethal osteogenesis imperfecta in twin pregnancy. Morin LR; Herlicoviez M; Loisel JC; Jacob B; Feuilly C; Stanescu V Clin Genet; 1991 Jun; 39(6):467-70. PubMed ID: 1863995 [TBL] [Abstract][Full Text] [Related]
14. Characterization of a type I collagen alpha 2(I) glycine-586 to valine substitution in osteogenesis imperfecta type IV. Detection of the mutation and prenatal diagnosis by a chemical cleavage method. Bateman JF; Hannagan M; Chan D; Cole WG Biochem J; 1991 Jun; 276 ( Pt 3)(Pt 3):765-70. PubMed ID: 2064612 [TBL] [Abstract][Full Text] [Related]
15. 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]
17. Consequences of an osteogenesis imperfecta diagnosis for survival and ambulation. Shapiro F J Pediatr Orthop; 1985; 5(4):456-62. PubMed ID: 4019761 [TBL] [Abstract][Full Text] [Related]
18. Multiexon deletion in an osteogenesis imperfecta variant with increased type III collagen mRNA. Chu ML; Gargiulo V; Williams CJ; Ramirez F J Biol Chem; 1985 Jan; 260(2):691-4. PubMed ID: 2981843 [TBL] [Abstract][Full Text] [Related]
19. [Prenatal diagnosis of osteogenesis imperfecta]. Barhmi R; Jacquemot C; el Rabiet G; Lasfargues P Rev Fr Gynecol Obstet; 1994 Dec; 89(12):613-6. PubMed ID: 7846469 [TBL] [Abstract][Full Text] [Related]