Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2012 | 2 |
2023 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
Types of Inheritance and Genes Associated with Familial Meniere Disease.
J Assoc Res Otolaryngol. 2023 Jun;24(3):269-279. doi: 10.1007/s10162-023-00896-0. Epub 2023 Apr 6.
J Assoc Res Otolaryngol. 2023.
PMID: 37022572
Free PMC article.
Review.
Meniere disease (MD) is a rare disorder of the inner ear defined by sensorineural hearing loss (SNHL) associated with episodes of vertigo and tinnitus. ...Familial MD shows different types of inheritance, including autosomal dominant and compound recessive …
Meniere disease (MD) is a rare disorder of the inner ear defined by sensorineural hearing loss (SNHL) associated with episodes …
Genetics of hearing and deafness.
Angeli S, Lin X, Liu XZ.
Angeli S, et al.
Anat Rec (Hoboken). 2012 Nov;295(11):1812-29. doi: 10.1002/ar.22579. Epub 2012 Oct 8.
Anat Rec (Hoboken). 2012.
PMID: 23044516
Free PMC article.
Review.
Most of the cases of genetic deafness recognized today are monogenic disorders that can be broadly classified by the mode of inheritance (i.e., autosomal dominant, autosomal recessive, X-linked, and mitochondrial inheritance) and by the presence of associated …
Most of the cases of genetic deafness recognized today are monogenic disorders that can be broadly classified by the mode of inheritance (i. …
Item in Clipboard
[Genetics of congenital deafness].
Faundes V, Pardo RA, Castillo Taucher S.
Faundes V, et al.
Med Clin (Barc). 2012 Oct 20;139(10):446-51. doi: 10.1016/j.medcli.2012.02.014. Epub 2012 Apr 24.
Med Clin (Barc). 2012.
PMID: 22538062
Review.
Spanish.
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. ...More than 400 syndromes accompanied of deafness have been described, which represent about 30% of cases of congenital hearing loss …
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. ... …
Item in Clipboard
Introduction to genetics for otorhinolaryngology nurses.
Malone KJ, Cook SS.
Malone KJ, et al.
ORL Head Neck Nurs. 2006 Spring;24(2):8-18.
ORL Head Neck Nurs. 2006.
PMID: 16696290
Review.
This article presents information about basic inheritance patterns (autosomal dominant and recessive, X-linked, and mitochondrial) and compares single-gene disorders to complex or mutifactorial diseases. Cleft lip and palate disorders (Robin sequence and Van der Wou …
This article presents information about basic inheritance patterns (autosomal dominant and recessive, X-linked, and mitochondr …
Item in Clipboard
Cite
Cite