155 related articles for article (PubMed ID: 7640757)
1. [Clinical heterogeneity of Townes-Brocks syndrome].
Parent P; Bensaid M; Le Guern H; Colin A; Broussine L; Chabarot A; Cozic A; Jehannin B; de Parscau L
Arch Pediatr; 1995 Jun; 2(6):551-4. PubMed ID: 7640757
[TBL] [Abstract][Full Text] [Related]
2. Townes-Brocks syndrome.
Priya ; Malhotra AK
Indian Pediatr; 2004 Jul; 41(7):743. PubMed ID: 15297694
[No Abstract] [Full Text] [Related]
3. Pierre Robin syndrome with caudal regression syndrome-a rare combination of congenital syndromes.
Ilyas M; Bashir I; Ellahi I; Shaheen F; Choh N
Childs Nerv Syst; 2018 Jun; 34(6):1105-1106. PubMed ID: 29651537
[No Abstract] [Full Text] [Related]
4. Two cases of Townes-Brocks syndrome.
Doray B; Langer B; Stoll C
Genet Couns; 1999; 10(4):359-67. PubMed ID: 10631923
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic and genotypic aspects of Townes-Brock syndrome: case report of patient in southern Brazil with a new SALL1 hotspot region nonsense mutation.
Liberalesso PBN; Cordeiro ML; Karuta SCV; Koladicz KRJ; Nitsche A; Zeigelboim BS; Raskin S; Rauchman M
BMC Med Genet; 2017 Nov; 18(1):125. PubMed ID: 29110636
[TBL] [Abstract][Full Text] [Related]
6. [Concomitant anomalies in developmental defects of the rectum and anus in children].
Arnaudov D; Apostolov A
Khirurgiia (Mosk); 1972 Jun; 48(6):99-100. PubMed ID: 4261346
[No Abstract] [Full Text] [Related]
7. High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial case.
Kohlhase J; Liebers M; Backe J; Baumann-Müller A; Bembea M; Destrée A; Gattas M; Grüssner S; Müller T; Mortier G; Skrypnyk C; Yano S; Wirbelauer J; Michaelis RC
J Med Genet; 2003 Nov; 40(11):e127. PubMed ID: 14627694
[No Abstract] [Full Text] [Related]
8. Townes-Brocks syndrome.
Powell CM; Michaelis RC
J Med Genet; 1999 Feb; 36(2):89-93. PubMed ID: 10051003
[TBL] [Abstract][Full Text] [Related]
9. Townes-Brocks syndrome in an infant with translocation t (5;16).
Serville F; Lacombe D; Saura R; Billeaud C; Sergent MP
Genet Couns; 1993; 4(2):109-12. PubMed ID: 8357560
[TBL] [Abstract][Full Text] [Related]
10. Accessory Auricles: Systematic Review of Definition, Associated Conditions, and Recommendations for Clinical Practice.
Amirhassankhani S; Lloyd MS
J Craniofac Surg; 2018 Mar; 29(2):372-375. PubMed ID: 29239919
[TBL] [Abstract][Full Text] [Related]
11. 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; 34(3):195-200. PubMed ID: 3180506
[TBL] [Abstract][Full Text] [Related]
12. Adult diagnosis of Townes-Brocks syndrome with renal failure: Two related cases and review of literature.
Beaudoux O; Lebre AS; Doco Fenzy M; Spodenkiewicz M; Canivet E; Colosio C; Poirsier C
Am J Med Genet A; 2021 Mar; 185(3):937-944. PubMed ID: 33438842
[TBL] [Abstract][Full Text] [Related]
13. [Hearing loss in Townes-Brocks syndrome].
Rodríguez Asensio J; Rodríguez Rosell MV; Ramos Pérez A
Acta Otorrinolaringol Esp; 2003; 54(7):518-22. PubMed ID: 14671925
[TBL] [Abstract][Full Text] [Related]
14. Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum.
Johnson JP; Poskanzer LS; Sherman S
Am J Med Genet; 1996 Jan; 61(2):134-9. PubMed ID: 8669439
[TBL] [Abstract][Full Text] [Related]
15. Rectal atresia as rare manifestation in EEC syndrome.
Majewski F; Goecke T
Am J Med Genet; 1996 May; 63(1):190-2. PubMed ID: 8723108
[TBL] [Abstract][Full Text] [Related]
16. Two coding single nucleotide polymorphisms in the SALL1 gene in Townes-Brocks syndrome: a case report and review of the literature.
Liang Y; Shen D; Cai W
J Pediatr Surg; 2008 Feb; 43(2):391-3. PubMed ID: 18280297
[TBL] [Abstract][Full Text] [Related]
17. SALL1 mutations in Townes-Brocks syndrome and related disorders.
Kohlhase J
Hum Mutat; 2000 Dec; 16(6):460-6. PubMed ID: 11102974
[TBL] [Abstract][Full Text] [Related]
18. 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; 111(2):230-1. PubMed ID: 12210359
[No Abstract] [Full Text] [Related]
19. Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects.
Kiefer SM; Ohlemiller KK; Yang J; McDill BW; Kohlhase J; Rauchman M
Hum Mol Genet; 2003 Sep; 12(17):2221-7. PubMed ID: 12915476
[TBL] [Abstract][Full Text] [Related]
20. Townes-Brocks syndrome with hypothyroidism.
Goswami V; Dubey NK
Indian Pediatr; 2007 Feb; 44(2):140-2. PubMed ID: 17351307
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]