Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1935 1
1961 2
1971 2
1973 2
1975 2
1976 1
1978 1
1979 4
1980 3
1981 1
1985 1
1987 2
1988 1
1989 1
1992 1
1993 2
1994 1
1995 2
1996 2
1997 2
1998 1
1999 1
2000 3
2001 1
2002 2
2003 2
2004 1
2005 1
2006 1
2007 1
2008 1
2011 1
2012 1
2013 2
2014 2
2016 1
2020 1
2021 2
2024 0

Text availability

Article attribute

Article type

Publication date

Similar articles for PMID: 8279480

57 results

Results by year

Filters applied: . Clear all
Page 1
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, Hussain K, Furth-Lavi J, Cosgrove KE, Shepherd RM, Barnes PD, O'Brien RE, Farndon PA, Sowden J, Liu XZ, Scanlan MJ, Malcolm S, Dunne MJ, Aynsley-Green A, Glaser B. Bitner-Glindzicz M, et al. Nat Genet. 2000 Sep;26(1):56-60. doi: 10.1038/79178. Nat Genet. 2000. PMID: 10973248
Hereditary renal-retinal dysplasia.
Godel V, Iaina A, Nemet P, Lazar M. Godel V, et al. Doc Ophthalmol. 1980 Oct 15;49(2):347-59. doi: 10.1007/BF01886626. Doc Ophthalmol. 1980. PMID: 7438990
57 results