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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
126 related items for PubMed ID: 5633139
1. Proximal symphalangism of fingers associated with fusion of os naviculare and talus and occurrence of two accessory bones in the feet (os paranaviculare and os tibiale externum) in an European--Indonesian--Chinese family. Wildervanck LS, Goedhard G, Meijer S. Acta Genet Stat Med; 1967; 17(1):166-77. PubMed ID: 5633139 [No Abstract] [Full Text] [Related]
2. [Radiological study of the accessory skeletal elements in the foot and ankle (author's transl)]. Tsuruta T, Shiokawa Y, Kato A, Matsumoto T, Yamazoe Y, Oike T, Sugiyama T, Saito M. Nihon Seikeigeka Gakkai Zasshi; 1981 Apr; 55(4):357-70. PubMed ID: 7276670 [Abstract] [Full Text] [Related]
3. Incidence of os tibiale externum in clinical pes planus. Wood WA, Spencer AM. J Am Podiatry Assoc; 1970 Jul; 60(7):276-9. PubMed ID: 5505626 [No Abstract] [Full Text] [Related]
4. Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a family. Drawbert JP, Stevens DB, Cadle RG, Hall BD. J Bone Joint Surg Am; 1985 Jul; 67(6):884-9. PubMed ID: 4019538 [Abstract] [Full Text] [Related]
5. Congenital malformation of the feet with low body height. A new syndrome, caused by an autosomal dominant gene. Gregersen HN, Petersen GB. Clin Genet; 1977 Nov; 12(5):255-62. PubMed ID: 589846 [Abstract] [Full Text] [Related]
6. Symphalangism with metacarpophalangeal fusions and elbow abnormalities. Kassner EG, Katz I, Qazi QH. Pediatr Radiol; 1976 Feb 13; 4(2):103-7. PubMed ID: 967566 [Abstract] [Full Text] [Related]
7. The congenital triangular deformity of the tubular bones of hand and foot. Jaeger M, Refior HJ. Clin Orthop Relat Res; 1971 Feb 13; 81():139-50. PubMed ID: 4332222 [No Abstract] [Full Text] [Related]
8. Camptobrachydactyly: a new autosomal dominant trait with two probable homozygotes. Edwards JA, Gale RP. Am J Hum Genet; 1972 Jul 13; 24(4):464-74. PubMed ID: 5031984 [No Abstract] [Full Text] [Related]
9. The EEC syndrome. Pries C, Mittelman D, Miller M, Solomon LM, Pashayan HM, Pruzansky S. Am J Dis Child; 1974 Jun 13; 127(6):840-4. PubMed ID: 4209740 [No Abstract] [Full Text] [Related]
10. Symphalangism (two phalanges) in the digits of the Japanese foot. Nakashima T, Hojo T, Suzuki K, Ijichi M. Ann Anat; 1995 May 13; 177(3):275-8. PubMed ID: 7598223 [Abstract] [Full Text] [Related]
11. [Distinctive features of the os naviculare pseudarthrosis vs the os naviculare accessorius]. Schuler MK, Dammann F, Schewe B, Winter E, Weise K. Unfallchirurg; 2003 Jan 13; 106(1):73-6. PubMed ID: 12552396 [Abstract] [Full Text] [Related]
12. Hereditary symphalangism with associated tarsal synostosis and hypophalangism. Castle JE, Bass S, Kanat IO. J Am Podiatr Med Assoc; 1993 Jan 13; 83(1):1-9. PubMed ID: 8419625 [Abstract] [Full Text] [Related]
13. [A case of endogenous familial hereditary malformation of both hands]. Brug E. Handchirurgie; 1975 Jan 13; 7(3):125-8. PubMed ID: 176087 [Abstract] [Full Text] [Related]
14. [Association of Wolff-Parkinson-White syndrome with congenital bone abnormalities of the hands and feet]. Gimenez VM, Trezza E. Arq Bras Cardiol; 1978 Dec 13; 31(6):399-401. PubMed ID: 751605 [No Abstract] [Full Text] [Related]
15. Beyond the obvious: Exploring Os Tibiale Externum and Os Peroneum in Foot and Ankle Pain - A Case Series. Yamajala S, Mane SS. J Orthop Case Rep; 2023 Mar 13; 13(3):44-49. PubMed ID: 37187822 [Abstract] [Full Text] [Related]
16. [Multiple synostosis]. Czeizel E, Göblyös P. Orv Hetil; 1993 Aug 29; 134(35):1917-20. PubMed ID: 8395675 [Abstract] [Full Text] [Related]
17. Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. Takahashi T, Takahashi I, Komatsu M, Sawaishi Y, Higashi K, Nishimura G, Saito H, Takada G. Clin Genet; 2001 Dec 29; 60(6):447-51. PubMed ID: 11846737 [Abstract] [Full Text] [Related]
18. A new nail dysplasia syndrome with onychonychia and absence and/or hypoplasia of distal phalanges. Cooks RG, Hertz M, Katznelson MB, Goodman RM. Clin Genet; 1985 Jan 29; 27(1):85-91. PubMed ID: 3978841 [Abstract] [Full Text] [Related]
19. Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3. Haberlandt E, Löffler J, Hirst-Stadlmann A, Stöckl B, Judmaier W, Fischer H, Heinz-Erian P, Müller T, Utermann G, Smith RJ, Janecke AR. J Med Genet; 2001 Jun 29; 38(6):405-9. PubMed ID: 11424924 [No Abstract] [Full Text] [Related]
20. A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability. Pang X, Luo H, Chai Y, Wang X, Sun L, He L, Chen P, Wu H, Yang T. PLoS One; 2015 Jun 29; 10(3):e0120816. PubMed ID: 25815513 [Abstract] [Full Text] [Related] Page: [Next] [New Search]