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4. Renal ultrasonography not required in babies with isolated minor ear anomalies. Deshpande SA; Watson H Arch Dis Child Fetal Neonatal Ed; 2006 Jan; 91(1):F29-30. PubMed ID: 16223753 [TBL] [Abstract][Full Text] [Related]
5. Renal anomalies and microtia: Determining the clinical utility of screening affected children. Kini S; Barton GW; Carol Liu YC Int J Pediatr Otorhinolaryngol; 2020 Jun; 133():109957. PubMed ID: 32109674 [TBL] [Abstract][Full Text] [Related]
8. Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders. Melnick M; Hodes ME; Nance WE; Yune H; Sweeney A Clin Genet; 1978 May; 13(5):425-42. PubMed ID: 657583 [TBL] [Abstract][Full Text] [Related]
9. Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies. Fraser FC; Ling D; Clogg D; Nogrady B Am J Med Genet; 1978; 2(3):241-52. PubMed ID: 263442 [TBL] [Abstract][Full Text] [Related]
10. [Branchio-oto-renal syndrome (BOR syndrome). A dysplasia syndrome with branchial abnormalities, deafness and kidney disease]. Holzmüller M HNO; 2000 Nov; 48(11):839-42. PubMed ID: 11139890 [TBL] [Abstract][Full Text] [Related]
11. Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndrome. Chitayat D; Hodgkinson KA; Chen MF; Haber GD; Nakishima S; Sando I Am J Med Genet; 1992 Aug; 43(6):970-5. PubMed ID: 1415348 [TBL] [Abstract][Full Text] [Related]
12. Congenital conductive or mixed deafness, preauricular sinus, external ear anomaly, and commissural lip pits: an autosomal dominant inherited syndrome. Marres HA; Cremers CW Ann Otol Rhinol Laryngol; 1991 Nov; 100(11):928-32. PubMed ID: 1746829 [TBL] [Abstract][Full Text] [Related]
13. The preauricular sinus: a review of its clinical presentation, treatment, and associations. Scheinfeld NS; Silverberg NB; Weinberg JM; Nozad V Pediatr Dermatol; 2004; 21(3):191-6. PubMed ID: 15165194 [TBL] [Abstract][Full Text] [Related]
14. Hemifacial microsomia and the branchio-oto-renal syndrome. Rollnick BR; Kaye CI J Craniofac Genet Dev Biol Suppl; 1985; 1():287-95. PubMed ID: 3877103 [TBL] [Abstract][Full Text] [Related]
15. Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients. Lehalle D; Gordon CT; Oufadem M; Goudefroye G; Boutaud L; Alessandri JL; Baena N; Baujat G; Baumann C; Boute-Benejean O; Caumes R; Decaestecker C; Gaillard D; Goldenberg A; Gonzales M; Holder-Espinasse M; Jacquemont ML; Lacombe D; Manouvrier-Hanu S; Marlin S; Mathieu-Dramard M; Morin G; Pasquier L; Petit F; Rio M; Smigiel R; Thauvin-Robinet C; Vasiljevic A; Verloes A; Malan V; Munnich A; de Pontual L; Vekemans M; Lyonnet S; Attié-Bitach T; Amiel J Hum Mutat; 2014 Apr; 35(4):478-85. PubMed ID: 24470203 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature. Senel E; Kocak H; Akbiyik F; Saylam G; Gulleroglu BN; Senel S J Pediatr Surg; 2009 Mar; 44(3):623-5. PubMed ID: 19302870 [TBL] [Abstract][Full Text] [Related]
18. Mild external ear malformations and renal tract abnormalities: a meta-analysis. Cuestas E; Bur C; Bongiovanni V Rev Fac Cien Med Univ Nac Cordoba; 2006; 63(1):46-52. PubMed ID: 17639808 [TBL] [Abstract][Full Text] [Related]
19. The BOR syndrome and renal agenesis--prenatal diagnosis and further clinical delineation. Greenberg CR; Trevenen CL; Evans JA Prenat Diagn; 1988 Feb; 8(2):103-8. PubMed ID: 3283716 [TBL] [Abstract][Full Text] [Related]
20. Prevalence of Renal and Cervical Vertebral Anomalies in Patients With Isolated Microtia and/or Aural Atresia. Zim S; Lee J; Rubinstein B; Senders C Cleft Palate Craniofac J; 2017 Nov; 54(6):664-667. PubMed ID: 27632762 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]