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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1960 | 1 |
1987 | 1 |
1988 | 1 |
1999 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 387857
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Congenital hereditary corneal dystrophy.
Am J Ophthalmol. 1960 Dec;50:1114-24. doi: 10.1016/0002-9394(60)90998-3.
Am J Ophthalmol. 1960.
PMID: 13768390
No abstract available.
Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
Hand CK, Harmon DL, Kennedy SM, FitzSimon JS, Collum LM, Parfrey NA.
Hand CK, et al.
Genomics. 1999 Oct 1;61(1):1-4. doi: 10.1006/geno.1999.5920.
Genomics. 1999.
PMID: 10512674
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Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.
Callaghan M, Hand CK, Kennedy SM, FitzSimon JS, Collum LM, Parfrey NA.
Callaghan M, et al.
Br J Ophthalmol. 1999 Jan;83(1):115-9. doi: 10.1136/bjo.83.1.115.
Br J Ophthalmol. 1999.
PMID: 10209448
Free PMC article.
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Congenital hereditary corneal oedema of Maumenee: its clinical features, management, and pathology.
Kirkness CM, McCartney A, Rice NS, Garner A, Steele AD.
Kirkness CM, et al.
Br J Ophthalmol. 1987 Feb;71(2):130-44. doi: 10.1136/bjo.71.2.130.
Br J Ophthalmol. 1987.
PMID: 3548808
Free PMC article.
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Comparison between posterior polymorphous dystrophy and congenital hereditary endothelial dystrophy of the cornea.
McCartney AC, Kirkness CM.
McCartney AC, et al.
Eye (Lond). 1988;2 ( Pt 1):63-70. doi: 10.1038/eye.1988.14.
Eye (Lond). 1988.
PMID: 3261696
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