These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3). Stratakis CA; Lin JP; Rennert OM Am J Med Genet; 1998 Sep; 79(3):209-14. PubMed ID: 9788564 [TBL] [Abstract][Full Text] [Related]
6. 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]
8. 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]
9. Familial branchio-oto-renal dysplasia: a new addition to the branchial arch syndromes. Melnick M; Bixler D; Nance WE; Silk K; Yune H Clin Genet; 1976 Jan; 9(1):25-34. PubMed ID: 1248162 [TBL] [Abstract][Full Text] [Related]
10. Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome. Kalatzis V; Sahly I; El-Amraoui A; Petit C Dev Dyn; 1998 Dec; 213(4):486-99. PubMed ID: 9853969 [TBL] [Abstract][Full Text] [Related]
11. Branchio-oto-renal dysplasia in three families. Gimsing S; Dyrmose J Ann Otol Rhinol Laryngol; 1986; 95(4 Pt 1):421-6. PubMed ID: 3740720 [TBL] [Abstract][Full Text] [Related]
12. Branchio-oto-renal dysplasia and branchio-oto dysplasia: report of eight new cases. Martini A; Comacchio F; Candiani F; Vio S Am J Otol; 1987 Mar; 8(2):116-22. PubMed ID: 3591918 [TBL] [Abstract][Full Text] [Related]
14. The earpits-deafness syndrome. Clinical and genetic aspects. Cremers CW; Fikkers-Van Noord M Int J Pediatr Otorhinolaryngol; 1980 Nov; 2(4):309-22. PubMed ID: 6964893 [TBL] [Abstract][Full Text] [Related]
15. Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree. König R; Fuchs S; Dukiet C Eur J Pediatr; 1994 Jun; 153(6):446-50. PubMed ID: 8088301 [TBL] [Abstract][Full Text] [Related]
16. Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome. Legius E; Fryns JP; Van den Berghe H Clin Genet; 1990 May; 37(5):347-50. PubMed ID: 2354548 [TBL] [Abstract][Full Text] [Related]
17. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13. Kumar S; Marres HA; Cremers CW; Kimberling WJ Am J Med Genet; 1998 Apr; 76(5):395-401. PubMed ID: 9556298 [TBL] [Abstract][Full Text] [Related]
18. [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]
19. Phenotypic manifestations of branchio-oto-renal syndrome. Chen A; Francis M; Ni L; Cremers CW; Kimberling WJ; Sato Y; Phelps PD; Bellman SC; Wagner MJ; Pembrey M Am J Med Genet; 1995 Sep; 58(4):365-70. PubMed ID: 8533848 [TBL] [Abstract][Full Text] [Related]
20. Syndromic ear anomalies and renal ultrasounds. Wang RY; Earl DL; Ruder RO; Graham JM Pediatrics; 2001 Aug; 108(2):E32. PubMed ID: 11483842 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]