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- Ferraz F. G., Nunes L., Ferraz M. E., Sousa J. P., 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] [Google Scholar]
- Hersh J. H., Jaworski M., Solinger R. E., Weisskopf B., Donat J. Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL association. Clin Pediatr (Phila) 1986 Feb;25(2):100–102. doi: 10.1177/000992288602500209. [DOI] [PubMed] [Google Scholar]
- Kurnit D. M., Steele M. W., 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. doi: 10.1016/s0022-3476(78)80518-6. [DOI] [PubMed] [Google Scholar]
- Monteiro de Pina-Neto J. Phenotypic variability in Townes-Brocks syndrome. Am J Med Genet. 1984 May;18(1):147–152. doi: 10.1002/ajmg.1320180118. [DOI] [PubMed] [Google Scholar]
- Naveh Y., Friedman A. Familial imperforate anus. Am J Dis Child. 1976 Apr;130(4):441–442. doi: 10.1001/archpedi.1976.02120050099020. [DOI] [PubMed] [Google Scholar]
- Pinsky L. The syndromology of anorectal malformation (atresia, stenosis, ectopia). Am J Med Genet. 1978;1(4):461–474. doi: 10.1002/ajmg.1320010408. [DOI] [PubMed] [Google Scholar]
- Reid I. S., Turner G. Familial and abnormality. J Pediatr. 1976 Jun;88(6):992–994. doi: 10.1016/s0022-3476(76)81061-x. [DOI] [PubMed] [Google Scholar]
- Schinzel A., Schmid W., Fraccaro M., Tiepolo L., Zuffardi O., Opitz J. M., Lindsten J., Zetterqvist P., Enell H., Baccichetti C. 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. doi: 10.1007/BF00282012. [DOI] [PubMed] [Google Scholar]
- Silver W., Steier M., Schwartz O., Zeichner M. B. The Holt-Oram syndrome with previously undescribed associated anomalies. Am J Dis Child. 1972 Dec;124(6):911–914. doi: 10.1001/archpedi.1972.02110180113017. [DOI] [PubMed] [Google Scholar]
- Spouge D., Baird P. A. Imperforate anus in 700,000 consecutive liveborn infants. Am J Med Genet Suppl. 1986;2:151–161. doi: 10.1002/ajmg.1320250619. [DOI] [PubMed] [Google Scholar]
- Townes P. L., Brocks E. R. Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies. J Pediatr. 1972 Aug;81(2):321–326. doi: 10.1016/s0022-3476(72)80302-0. [DOI] [PubMed] [Google Scholar]
- Walpole I. R., Hockey A. Syndrome of imperforate anus, abnormalities of hands and feet, satyr ears, and sensorineural deafness. J Pediatr. 1982 Feb;100(2):250–252. doi: 10.1016/s0022-3476(82)80649-5. [DOI] [PubMed] [Google Scholar]
- Weaver D. D., Mapstone C. L., Yu P. L. The VATER association. Analysis of 46 patients. Am J Dis Child. 1986 Mar;140(3):225–229. doi: 10.1001/archpedi.1986.02140170051027. [DOI] [PubMed] [Google Scholar]
- de Vries-Van der Weerd M. A., Willems P. J., Mandema H. M., ten Kate L. P. A new family with the Townes-Brocks syndrome. Clin Genet. 1988 Sep;34(3):195–200. doi: 10.1111/j.1399-0004.1988.tb02862.x. [DOI] [PubMed] [Google Scholar]