| J Med Genet. 1990 July; 27(7): 457–461. | PMCID: PMC1017185 |
The Townes-Brocks syndrome. M O'Callaghan and I D Young Department of Child Health, Leicester Royal Infirmary. Full text Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (1011K), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References. Images in this article Click on the image to see a larger version. These references are in PubMed. This may not be the complete list of references from this article. - Townes, PL; Brocks, ER. Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies. J Pediatr. 1972 Aug;81(2):321–326. [PubMed]
- Reid, IS; Turner, G. Familial and abnormality. J Pediatr. 1976 Jun;88(6):992–994. [PubMed]
- Kurnit, DM; Steele, MW; Pinsky, L; Dibbins, A. Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformations. J Pediatr. 1978 Aug;93(2):270–273. [PubMed]
- Walpole, IR; Hockey, A. Syndrome of imperforate anus, abnormalities of hands and feet, satyr ears, and sensorineural deafness. J Pediatr. 1982 Feb;100(2):250–252. [PubMed]
- de Vries-Van der Weerd, MA; Willems, PJ; Mandema, HM; ten Kate, LP. A new family with the Townes-Brocks syndrome. Clin Genet. 1988 Sep;34(3):195–200. [PubMed]
- Monteiro de Pina-Neto, J. Phenotypic variability in Townes-Brocks syndrome. Am J Med Genet. 1984 May;18(1):147–152. [PubMed]
- Hersh, JH; Jaworski, M; Solinger, RE; Weisskopf, B; Donat, J. Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL association. Clin Pediatr (Phila). 1986 Feb;25(2):100–102. [PubMed]
- Ferraz, FG; Nunes, L; Ferraz, ME; Sousa, JP; Santos, M; Carvalho, C; Maroteaux, P. Townes-Brocks syndrome. Report of a case and review of the literature. Ann Genet. 1989;32(2):120–123. [PubMed]
- Spouge, D; Baird, PA. Imperforate anus in 700,000 consecutive liveborn infants. Am J Med Genet Suppl. 1986;2:151–161. [PubMed]
- Pinsky, L. The syndromology of anorectal malformation (atresia, stenosis, ectopia). Am J Med Genet. 1978;1(4):461–474. [PubMed]
- Weaver, DD; Mapstone, CL; Yu, PL. The VATER association. Analysis of 46 patients. Am J Dis Child. 1986 Mar;140(3):225–229. [PubMed]
- Naveh, Y; Friedman, A. Familial imperforate anus. Am J Dis Child. 1976 Apr;130(4):441–442. [PubMed]
- Silver, W; Steier, M; Schwartz, O; Zeichner, MB. The Holt-Oram syndrome with previously undescribed associated anomalies. Am J Dis Child. 1972 Dec;124(6):911–914. [PubMed]
- Schinzel, A; Schmid, W; Fraccaro, M; Tiepolo, L; Zuffardi, O; Opitz, JM; Lindsten, J; Zetterqvist, P; Enell, H; Baccichetti, C; Tenconi, R; Pagon, RA. The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture. Hum Genet. 1981;57(2):148–158. [PubMed]
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