157 related articles for article (PubMed ID: 7515752)
1. A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents.
al Gazali LI; Sabrinathan K; Nair KG
Clin Dysmorphol; 1994 Jan; 3(1):55-62. PubMed ID: 7515752
[TBL] [Abstract][Full Text] [Related]
2. Osteogenesis imperfecta type IIA: evidence for dominant inheritance.
Young ID; Thompson EM; Hall CM; Pembrey ME
J Med Genet; 1987 Jul; 24(7):386-9. PubMed ID: 3612714
[TBL] [Abstract][Full Text] [Related]
3. Wormian bones in osteogenesis imperfecta and other disorders.
Cremin B; Goodman H; Spranger J; Beighton P
Skeletal Radiol; 1982; 8(1):35-8. PubMed ID: 7079781
[TBL] [Abstract][Full Text] [Related]
4. Homozygous osteogenesis imperfecta unlinked to collagen I genes.
Aitchison K; Ogilvie D; Honeyman M; Thompson E; Sykes B
Hum Genet; 1988 Mar; 78(3):233-6. PubMed ID: 2894346
[TBL] [Abstract][Full Text] [Related]
5. Osteogenesis imperfecta-like syndrome with severe mental retardation and extrapyramidal tract signs.
Nishimura G; Kurosawa K; Kobayashi H; Kawame H
Pediatr Radiol; 1998 Nov; 28(11):856-8. PubMed ID: 9799318
[TBL] [Abstract][Full Text] [Related]
6. [Clinical picture and genetics of osteogenesis imperfecta].
Langness U; Behnke H
Dtsch Med Wochenschr; 1970 Jan; 95(5):209-12 passim. PubMed ID: 5410905
[No Abstract] [Full Text] [Related]
7. Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?
al Gazali LI; al Talabani J; Mosawi A; Lytle W
Clin Dysmorphol; 1994 Jul; 3(3):238-44. PubMed ID: 7981860
[TBL] [Abstract][Full Text] [Related]
8. Osteogenesis imperfecta with joint contractures: bruck syndrome.
Blacksin MF; Pletcher BA; David M
Pediatr Radiol; 1998 Feb; 28(2):117-9. PubMed ID: 9472060
[TBL] [Abstract][Full Text] [Related]
9. Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations.
Aldinger KA; Mendelsohn NJ; Chung BH; Zhang W; Cohn DH; Fernandez B; Alkuraya FS; Dobyns WB; Curry CJ
J Med Genet; 2016 Jun; 53(6):427-30. PubMed ID: 26671912
[No Abstract] [Full Text] [Related]
10. [Osteogenesis imperfecta (author's transl)].
Zergollern L; Depeder Z; Stakić A; Rezić P
Lijec Vjesn; 1976 Aug; 98(8):412-8. PubMed ID: 1004092
[No Abstract] [Full Text] [Related]
11. [Case of congenital osteogenesis imperfecta].
Ambrosiani S; Brignone S
Minerva Med; 1973 Oct; 64(70):3660-6. PubMed ID: 4767746
[No Abstract] [Full Text] [Related]
12. [Osteogenesis imperfecta].
Bol Med Hosp Infant Mex; 1981; 38(2):363-78. PubMed ID: 7259853
[No Abstract] [Full Text] [Related]
13. Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity.
Sillence DO; Barlow KK; Garber AP; Hall JG; Rimoin DL
Am J Med Genet; 1984 Feb; 17(2):407-23. PubMed ID: 6702894
[TBL] [Abstract][Full Text] [Related]
14. Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome.
Roifman CM; Chitayat D
Clin Genet; 2009 Nov; 76(5):449-57. PubMed ID: 19863561
[TBL] [Abstract][Full Text] [Related]
15. [Heterogeneity in osteogenesis imperfecta].
Zergollern L; Barisić I; Zergollern S
Acta Med Iugosl; 1988; 42(2):115-31. PubMed ID: 3389192
[No Abstract] [Full Text] [Related]
16. [Congenital osteogenesis imperfecta diagnosed in utero. Report of a case].
Kehler M
Ugeskr Laeger; 1974 Jun; 136(24):1302-3. PubMed ID: 4840260
[No Abstract] [Full Text] [Related]
17. Bruck syndrome: neonatal presentation and natural course in three patients.
Leroy JG; Nuytinck L; De Paepe A; De Rammelaere M; Gillerot Y; Verloes A; Loeys B; De Groote W
Pediatr Radiol; 1998 Oct; 28(10):781-9. PubMed ID: 9799301
[TBL] [Abstract][Full Text] [Related]
18. Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation.
Nwosu BU; Raygada M; Tsilou ET; Rennert OM; Stratakis CA
Ophthalmic Genet; 2005 Sep; 26(3):135-8. PubMed ID: 16272059
[TBL] [Abstract][Full Text] [Related]
19. [Osteogenesis imperfecta diagnoses early, apropos of a case at the Yalgadou Ouédraogo National Hospital Center of Ouagadougou].
Cisse R; Tapsoba TL; Lankoande J; Zeba B; Bamouni AY; Sakande B; Sano D; Wandaogo A; Ouedraogo B; Sawadogo A
Dakar Med; 1998; 43(1):132-4. PubMed ID: 9827173
[TBL] [Abstract][Full Text] [Related]
20. Osteogenesis imperfecta: report of 2 cases.
Bradley FJ; Essex T
J Am Osteopath Assoc; 1985 Jul; 85(7):462-6. PubMed ID: 3900017
[No Abstract] [Full Text] [Related]
[Next] [New Search]