69 related articles for article (PubMed ID: 906107)
1. [Hereditary peripheral epi-diaphyseal dysostosis. Report of a case of atypical peripheral dysostosis].
Frandsen PJ
Ugeskr Laeger; 1977 Aug; 139(32):1909-10. PubMed ID: 906107
[No Abstract] [Full Text] [Related]
2. [The cone-shaped epiphyses of the hands and feet (peripheral dysostosis].
LIESS G
Fortschr Geb Rontgenstr; 1954 Aug; 81(2):173-81. PubMed ID: 13200642
[No Abstract] [Full Text] [Related]
3. Angel-shaped phalango-epiphyseal dysplasia (ASPED): identification of a new genetic bone marker.
Giedion A; Prader A; Fliegel C; Krasikov N; Langer L; Poznanski A
Am J Med Genet; 1993 Oct; 47(5):765-71. PubMed ID: 8267010
[TBL] [Abstract][Full Text] [Related]
4. Unusual multiple epiphyseal dysplasias.
Lie SO; Siggers DC; Dorst JP; Kopits SE
Birth Defects Orig Artic Ser; 1974; 10(12):165-85. PubMed ID: 4461058
[No Abstract] [Full Text] [Related]
5. Bilateral asymmetry in cone epiphysis of the middle phalanx, fifth finger.
Wetherington RK
Am J Phys Anthropol; 1983 Mar; 60(3):319-21. PubMed ID: 6846506
[TBL] [Abstract][Full Text] [Related]
6. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
[No Abstract] [Full Text] [Related]
7. Multiple epiphyseal dysplasia. Report of a pedigree.
Murphy MC; Shine IB; Stevens DB
J Bone Joint Surg Am; 1973 Jun; 55(4):814-20. PubMed ID: 4283754
[No Abstract] [Full Text] [Related]
8. A family with diaphyseal aclasis and peripheral dysostosis.
Brooks AP; Wynne-Davies R
J Med Genet; 1980 Aug; 17(4):277-80. PubMed ID: 7205902
[TBL] [Abstract][Full Text] [Related]
9. [Tricho-rhino-phalangeal syndrome. Four family cases].
Cottin S; Le Gall G; Lorgeas JM
Rev Rhum Mal Osteoartic; 1980 Mar; 47(3):169-73. PubMed ID: 7384726
[TBL] [Abstract][Full Text] [Related]
10. [Diastrophic dwarfism or "metaphyseal dysostosis"].
Fauchier C; Régy JM; Combe P
Ann Pediatr (Paris); 1970 Dec; 17(12):876-81. PubMed ID: 4993571
[No Abstract] [Full Text] [Related]
11. New manifestations observed in the Tel Hashomer camptodactyly syndrome.
Gollop T; Dal Colletto GM; Ferraretto I; Grimaldi A
Prog Clin Biol Res; 1982; 104():269-77. PubMed ID: 7163271
[No Abstract] [Full Text] [Related]
12. [Trichorhinophalangeal syndrome (Giedion)].
Ferrando J; Del Olmo JA; Bassas J; Fernández E; Fontarnau R
Med Cutan Ibero Lat Am; 1981; 9(5):351-60. PubMed ID: 7038349
[TBL] [Abstract][Full Text] [Related]
13. [Bone dysplasia with dwarfism and diffuse skeletal alterations].
Piussan C; Maroteaux P; Castroviejo I; Risbourg B
Arch Fr Pediatr; 1975; 32(6):541-50. PubMed ID: 1080993
[TBL] [Abstract][Full Text] [Related]
14. [Ainhum in Eritrea. Description of a case associated with a picture of Brailsford's peripheral dysostosis].
Mara M; Tresca G
Arch Ital Sci Med Trop Parassitol; 1965; 46(11):453-60. PubMed ID: 5859839
[No Abstract] [Full Text] [Related]
15. [Ossification in brachydactyly].
Köster D
Beitr Orthop Traumatol; 1971 May; 18(5):271-80. PubMed ID: 5000149
[No Abstract] [Full Text] [Related]
16. [Craniofacial dysostosis with diaphyseal hyperplasia].
Maximilian C; Dumitriu L; Ioanitiu D; Ispas I; Firu P; Ciovirnache M; Duca D
J Genet Hum; 1981 Jun; 29(2):129-39. PubMed ID: 7328407
[TBL] [Abstract][Full Text] [Related]
17. The trichorhinophalangeal syndrome. Report of 4 familial cases belonging to 4 generations.
Ferrández A; Remírez J; Sáenz P; Calvo M
Helv Paediatr Acta; 1980 Dec; 35(6):559-67. PubMed ID: 7204100
[TBL] [Abstract][Full Text] [Related]
18. The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family.
Gollop TR; Colletto GM
Am J Med Genet; 1984 Feb; 17(2):399-406. PubMed ID: 6702893
[TBL] [Abstract][Full Text] [Related]
19. Cone-shaped epiphyses of the hands and their diagnostic value. The tricho-rhino-phalangeal syndrome.
Giedion A
Ann Radiol (Paris); 1967; 10(3):322-9. PubMed ID: 6051973
[No Abstract] [Full Text] [Related]
20. Growth hormone deficiency, wormian bones, dextrocardia, brachycamptodactyly, and other midline defects.
Stratton RF; Parker MW
Am J Med Genet; 1989 Feb; 32(2):169-73. PubMed ID: 2564736
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
