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6. Familial microtia with meatal atresia and conductive deafness in five generations. Gupta A, Patton MA. Am J Med Genet; 1995 Nov 06; 59(2):238-41. PubMed ID: 8588593 [Abstract] [Full Text] [Related]
12. 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 06; 13(5):425-42. PubMed ID: 657583 [Abstract] [Full Text] [Related]
13. 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 13; 76(5):395-401. PubMed ID: 9556298 [Abstract] [Full Text] [Related]
14. [Branchio-oto-renal syndrome (BOR syndrome). A dysplasia syndrome with branchial abnormalities, deafness and kidney disease]. Holzmüller M. HNO; 2000 Nov 13; 48(11):839-42. PubMed ID: 11139890 [Abstract] [Full Text] [Related]
15. Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome? Fraser FC, Aymé S, Halal F, Sproule J. Am J Med Genet; 1983 Mar 13; 14(3):473-8. PubMed ID: 6859100 [Abstract] [Full Text] [Related]
16. 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 23; 79(3):209-14. PubMed ID: 9788564 [Abstract] [Full Text] [Related]
19. Johnson-McMillin syndrome: report of a new case with novel features. Cushman LJ, Torres-Martinez W, Weaver DD. Birth Defects Res A Clin Mol Teratol; 2005 Sep 23; 73(9):638-41. PubMed ID: 16116593 [Abstract] [Full Text] [Related]