129 related articles for article (PubMed ID: 4600478)
1. [Symphalangism, strabism, and anomaly of the middle ear (author's transl)].
Gloede JF; Stenger HH
Humangenetik; 1974 Apr; 22(1):23-32. PubMed ID: 4600478
[No Abstract] [Full Text] [Related]
2. [Multiple synostosis].
Czeizel E; Göblyös P
Orv Hetil; 1993 Aug; 134(35):1917-20. PubMed ID: 8395675
[TBL] [Abstract][Full Text] [Related]
3. Stapes fixation a proximal symphalangism.
Gorlin RJ; Kietzer G; Wolfson J
Z Kinderheilkd; 1970; 108(1):12-6. PubMed ID: 5440467
[No Abstract] [Full Text] [Related]
4. Brachydactyly type C associated with shortening of the hallux.
Rowe-Jones JM; Moss AL; Patton MA
J Med Genet; 1992 May; 29(5):346-8. PubMed ID: 1583664
[TBL] [Abstract][Full Text] [Related]
5. The Robinow syndrome: an isolated case with a detailed study of the phenotype.
Kelly TE; Benson R; Temtamy S; Plotnick L; Levin S
Am J Dis Child; 1975 Mar; 129(3):383-6. PubMed ID: 1121970
[No Abstract] [Full Text] [Related]
6. [Weill-Marchesani's syndrome (author's transl)].
Ramos Niembro F; Zavala C
Rev Invest Clin; 1975; 27(3):225-30. PubMed ID: 1188208
[No Abstract] [Full Text] [Related]
7. A syndrome of polydactyly-syndactyly and triphalangeal thumbs in three generations.
Yujnovsky O; Ayala D; Vincitorio A; Viale H; Sakati N; Nyhan WL
Clin Genet; 1974; 6(1):51-9. PubMed ID: 4372010
[No Abstract] [Full Text] [Related]
8. [Symphalangism (author's transl)].
Seigneuric C; Serrad E; Cortet P; Mabille JP
Ann Radiol (Paris); 1982 Mar; 25(3):213-6. PubMed ID: 7092112
[No Abstract] [Full Text] [Related]
9. [Symphalangism (author's transl)].
Szmurło J; Jakubowski K
Pol Przegl Radiol Med Nukl; 1979; 43(1):25-8. PubMed ID: 450741
[No Abstract] [Full Text] [Related]
10. A particular form of cranio-facio-mandibular dysostosis with type B brachydactylia.
Van Damme W; Touitou D
J Belge Radiol; 1980; 63(4):491-6. PubMed ID: 7204325
[No Abstract] [Full Text] [Related]
11. Dominant symphalangism and conductive hearing loss.
Makowski A; Latkowski B; Niebudek-Bogusz E
Rev Laryngol Otol Rhinol (Bord); 1995; 116(5):339-40. PubMed ID: 8677370
[TBL] [Abstract][Full Text] [Related]
12. [A case of dwarfism with oto-palato-digital involvement (author's transl)].
Farriaux JP; Dubois O; Maroteaux P; Fontaine G
J Radiol Electrol Med Nucl; 1974 Feb; 55(2):137-42. PubMed ID: 4408413
[No Abstract] [Full Text] [Related]
13. Anophthalmia, multiple abnormalities, and unusual karyotype.
Masket S; Galioto FM; Best M
Am J Ophthalmol; 1970 Sep; 70(3):381-3. PubMed ID: 4915926
[No Abstract] [Full Text] [Related]
14. Cone-shaped epiphyses in the distal phalanges. Case report of a child with anorchia.
Saldino RM; Marshall S; Taybi H
Radiol Clin Biol; 1972; 41(6):449-52. PubMed ID: 4404981
[No Abstract] [Full Text] [Related]
15. Hereditary symphalangism with associated tarsal synostosis and hypophalangism.
Castle JE; Bass S; Kanat IO
J Am Podiatr Med Assoc; 1993 Jan; 83(1):1-9. PubMed ID: 8419625
[TBL] [Abstract][Full Text] [Related]
16. Triphalangeal thumbs-ectrodactyly in a sporadic case.
Majewski F; Kemperdick H; Goecke T
Clin Genet; 1981 Oct; 20(4):310-4. PubMed ID: 7333024
[No Abstract] [Full Text] [Related]
17. Coexisting ectrodacytyly-ectodermal dysplasia-clefting (EEC) and prune belly syndromes. Report of a case.
Ivarsson S; Henriksson P; Theander G
Acta Radiol Diagn (Stockh); 1982; 23(3B):287-92. PubMed ID: 7148490
[No Abstract] [Full Text] [Related]
18. Brachydactylia with symphalangism, probably autosomal recessive.
Walbaum R; Hazard C; Cordier R
Hum Genet; 1976 Jul; 33(2):189-92. PubMed ID: 939572
[TBL] [Abstract][Full Text] [Related]
19. Opitz trigonocephaly syndrome and terminal transverse limb reduction defects.
Fryns JP; Snoeck L; Kleczkowska A; Van den Berghe H
Helv Paediatr Acta; 1985; 40(6):485-8. PubMed ID: 3830973
[TBL] [Abstract][Full Text] [Related]
20. Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritis.
Ventruto V; Di Girlamo R; Festa B; Romano A; Sebastio G; Sebastio L
J Med Genet; 1976 Oct; 13(5):394-8. PubMed ID: 1003450
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
