134 related articles for article (PubMed ID: 4641184)
1. Roentgenographic findings in familial osteodysplasia.
Buchignani JS; Cook AJ; Anderson LG
Am J Roentgenol Radium Ther Nucl Med; 1972 Nov; 116(3):602-8. PubMed ID: 4641184
[No Abstract] [Full Text] [Related]
2. Frontometaphyseal dysplasia.
Holt JF; Thompson GR; Arenberg IK
Radiol Clin North Am; 1972 Aug; 10(2):225-43. PubMed ID: 5044403
[No Abstract] [Full Text] [Related]
3. An unusual familial spondyloepiphyseal dysplasia: "spondyloperipheral dysplasia".
Kelly TE; Lichtenstein JR; Dorst JP
Birth Defects Orig Artic Ser; 1977; 13(3B):149-65. PubMed ID: 407956
[No Abstract] [Full Text] [Related]
4. Progessive diaphyseal dysplasia. Review of the literature and report of seven cases in one family.
Hundley JD; Wilson FC
J Bone Joint Surg Am; 1973 Apr; 55(3):461-74. PubMed ID: 4703201
[No Abstract] [Full Text] [Related]
5. [Case of craniometaphyseal dysplasia considered to be typical in x-ray figures].
Katsumata N; Tanabe M; Aono K; Morino Y; Watanabe S
Rinsho Hoshasen; 1971 Aug; 16(8):637-42. PubMed ID: 5209368
[No Abstract] [Full Text] [Related]
6. A case of autosomal recessive form of cranio-metaphyseal dysplasia with unusual features and with bone fragility.
Ventruto V; Ametrano O; D'Avanzo G; Della Bruna M; Stabile M; Lonardo F; Marasca F; Tortora P
Australas Radiol; 1987 Feb; 31(1):79-82. PubMed ID: 3619813
[No Abstract] [Full Text] [Related]
7. Roentgenographic findings in fucosidosis type 2.
Brill PW; Beratis NG; Kousseff BG; Hirschhorn K
Am J Roentgenol Radium Ther Nucl Med; 1975 May; 124(1):75-82. PubMed ID: 167599
[TBL] [Abstract][Full Text] [Related]
8. Precocious type of osteodysplasia. A new autosomal recessive form.
Kozlowski K; Mayne V; Danks DM
Acta Radiol Diagn (Stockh); 1973 Mar; 14(2):171-6. PubMed ID: 4727256
[No Abstract] [Full Text] [Related]
9. Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
Gall JC; Stern AM; Poznanski AK; Garn SM; Weinstein ED; Hayward JR
Am J Hum Genet; 1972 Jan; 24(1):24-36. PubMed ID: 5012690
[No Abstract] [Full Text] [Related]
10. A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet.
Eiken M; Prag J; Petersen KE; Kaufmann HJ
Eur J Pediatr; 1984 Feb; 141(4):231-5. PubMed ID: 6734674
[TBL] [Abstract][Full Text] [Related]
11. A bone dysplasia with deafness.
Insley J; Astley R
Br J Radiol; 1974 May; 47(557):244-51. PubMed ID: 4830146
[No Abstract] [Full Text] [Related]
12. Familial osteodysplasia.
Anderson LG; Cook AJ; Coccaro PJ; Coro CJ; Bosma JF
JAMA; 1972 Jun; 220(13):1687-93. PubMed ID: 5067603
[No Abstract] [Full Text] [Related]
13. Osseous changes of osteopathia striata and Pyle's disease occurring in a patient with an 11 year follow-up. A case report.
Culver GJ; Thumasathit C
Am J Roentgenol Radium Ther Nucl Med; 1972 Nov; 116(3):640-3. PubMed ID: 4641188
[No Abstract] [Full Text] [Related]
14. Trisomy 9p, a chromosome aberration with distinct radiologic findings.
Schinzel A
Radiology; 1979 Jan; 130(1):125-33. PubMed ID: 758640
[TBL] [Abstract][Full Text] [Related]
15. [X-ray figures in Dl trisomy syndrome].
Watanabe T; Mita M; Osawa T; Fujimoto S
Rinsho Hoshasen; 1971 Aug; 16(8):643-8. PubMed ID: 5209369
[No Abstract] [Full Text] [Related]
16. An autosomal recessive bone dysplasia syndrome resembling hypochondroplasia.
Desch LW; Horton WA
Pediatrics; 1985 Apr; 75(4):786-9. PubMed ID: 4039054
[No Abstract] [Full Text] [Related]
17. A "calcified suprasellar mass" in association with spondylometaphyseal dysplasia.
Strand RD; Green B
Ann Radiol (Paris); 1974; 17(4):369-74. PubMed ID: 4447311
[No Abstract] [Full Text] [Related]
18. Roentgenographic manifestations of Leroy's I-cell disease.
Taber P; Gyepes MT; Philippart M; Ling S
Am J Roentgenol Radium Ther Nucl Med; 1973 May; 118(1):213-21. PubMed ID: 4267400
[No Abstract] [Full Text] [Related]
19. Sjögren-Larsson syndrome with epiphyseal-metaphyseal dysplasia.
Ozonoff MB; Ogden JA
Am J Roentgenol Radium Ther Nucl Med; 1973 May; 118(1):187-92. PubMed ID: 4634106
[No Abstract] [Full Text] [Related]
20. Radiological features of the most common autosomal disorders: trisomy 21-22 (mongolism or Down's syndrome), trisomy 18, trisomy 13-15, and the cri du chat syndrome.
James AE; Merz T; Janower ML; Dorst JP
Clin Radiol; 1971 Oct; 22(4):417-33. PubMed ID: 4257566
[No Abstract] [Full Text] [Related]
[Next] [New Search]