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3. Somatic mosaicism and variable expression of Townes-Brocks syndrome. Devriendt K, Fryns JP, Lemmens F, Kohlhase J, Liebers M. Am J Med Genet; 2002 Aug 01; 111(2):230-1. PubMed ID: 12210359 [No Abstract] [Full Text] [Related]
4. Townes-Brocks syndrome. Report of a case and review of the literature. Ferraz FG, Nunes L, Ferraz ME, Sousa JP, Santos M, Carvalho C, Maroteaux P. Ann Genet; 1989 Aug 01; 32(2):120-3. PubMed ID: 2667456 [Abstract] [Full Text] [Related]
5. [The Townes-Brocks syndrome]. Arroyo Carrera I, López Cuesta MJ, García García MJ, Lozano Rodríguez JA, Carretero Díaz V. An Esp Pediatr; 1996 Apr 01; 44(4):364-6. PubMed ID: 8849089 [No Abstract] [Full Text] [Related]
6. Two cases of Townes-Brocks syndrome with previously undescribed anomalies. Marlin S, Toublanc JE, Petit C. Clin Dysmorphol; 1998 Oct 01; 7(4):295-8. PubMed ID: 9823498 [Abstract] [Full Text] [Related]
8. Townes-Brocks syndrome with hypothyroidism. Goswami V, Dubey NK. Indian Pediatr; 2007 Feb 01; 44(2):140-2. PubMed ID: 17351307 [Abstract] [Full Text] [Related]
9. [Comments on the contribution by D. Kotzot et al. Townes-Brocks syndrome]. Lenz W. Monatsschr Kinderheilkd; 1993 Oct 01; 141(10):791-2. PubMed ID: 8264682 [No Abstract] [Full Text] [Related]
10. Phenotypic variability in Townes-Brocks syndrome. Monteiro de Pina-Neto J. Am J Med Genet; 1984 May 01; 18(1):147-52. PubMed ID: 6741990 [Abstract] [Full Text] [Related]
11. Two cases of Townes-Brocks syndrome. Doray B, Langer B, Stoll C. Genet Couns; 1999 May 01; 10(4):359-67. PubMed ID: 10631923 [Abstract] [Full Text] [Related]
12. Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient. Marlin S, Blanchard S, Slim R, Lacombe D, Denoyelle F, Alessandri JL, Calzolari E, Drouin-Garraud V, Ferraz FG, Fourmaintraux A, Philip N, Toublanc JE, Petit C. Hum Mutat; 1999 May 01; 14(5):377-86. PubMed ID: 10533063 [Abstract] [Full Text] [Related]
13. A new family with the Townes-Brocks syndrome. de Vries-Van der Weerd MA, Willems PJ, Mandema HM, ten Kate LP. Clin Genet; 1988 Sep 01; 34(3):195-200. PubMed ID: 3180506 [Abstract] [Full Text] [Related]
15. Townes-Brocks syndrome in an infant with translocation t (5;16). Serville F, Lacombe D, Saura R, Billeaud C, Sergent MP. Genet Couns; 1993 Sep 01; 4(2):109-12. PubMed ID: 8357560 [Abstract] [Full Text] [Related]
16. [Townes-Brocks syndrome (anus, hand and ear syndrome). A case report]. Pisi P, Orlandi PE, Santoli G, Imbriani M, Balzi F. Radiol Med; 1995 Sep 01; 89(1-2):173-5. PubMed ID: 7716304 [No Abstract] [Full Text] [Related]
17. [A triphalangeal thumb associated with otological abnormalities. A new syndrome?]. Raia V, Strisciuglio P, Andolfi M, Paludetto R. Pediatr Med Chir; 1987 Sep 01; 9(5):611-2. PubMed ID: 3441436 [Abstract] [Full Text] [Related]
18. [Hearing loss in Townes-Brocks syndrome]. Rodríguez Asensio J, Rodríguez Rosell MV, Ramos Pérez A. Acta Otorrinolaringol Esp; 2003 Sep 01; 54(7):518-22. PubMed ID: 14671925 [Abstract] [Full Text] [Related]
19. Association of a de novo 16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes. Bardakjian TM, Schneider AS, Ng D, Johnston JJ, Biesecker LG. BMC Med Genet; 2009 Dec 16; 10():137. PubMed ID: 20003547 [Abstract] [Full Text] [Related]
20. Townes-Brocks syndrome. König R, Schick U, Fuchs S. Eur J Pediatr; 1990 Dec 16; 150(2):100-3. PubMed ID: 2279502 [Abstract] [Full Text] [Related] Page: [Next] [New Search]