Oley CA[au] - Search Results

Year	Number of Results
1986	1
1988	1
1989	1
1990	1
1992	2
1993	1
1994	1
1995	1
1996	1
1997	1
2000	1
2002	1
2024	0

1

Wong VA, Beckingsale PS, Oley CA, Sullivan TJ. Wong VA, et al. Among authors: oley ca. Ophthalmology. 2002 May;109(5):1023-31. doi: 10.1016/s0161-6420(02)01009-6. Ophthalmology. 2002. PMID: 11986113

2

A reappraisal of the CHARGE association.

Oley CA, Baraitser M, Grant DB. Oley CA, et al. J Med Genet. 1988 Mar;25(3):147-56. doi: 10.1136/jmg.25.3.147. J Med Genet. 1988. PMID: 3351900 Free PMC article.

3

Three-generation transmission of Hirschsprung's disease.

Lipson AH, Harvey J, Oley CA. Lipson AH, et al. Among authors: oley ca. Clin Genet. 1990 Mar;37(3):235. doi: 10.1111/j.1399-0004.1990.tb03509.x. Clin Genet. 1990. PMID: 2323095 No abstract available.

4

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

Parker WD Jr, Oley CA, Parks JK. Parker WD Jr, et al. Among authors: oley ca. N Engl J Med. 1989 May 18;320(20):1331-3. doi: 10.1056/NEJM198905183202007. N Engl J Med. 1989. PMID: 2497346 No abstract available.

5

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes.

Walker AP, Chelly J, Love DR, Brush YI, Récan D, Chaussain JL, Oley CA, Connor JM, Yates J, Price DA, et al. Walker AP, et al. Among authors: oley ca. Hum Mol Genet. 1992 Nov;1(8):579-85. doi: 10.1093/hmg/1.8.579. Hum Mol Genet. 1992. PMID: 1301166

6

Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases.

Hargrave M, James K, Nield K, Toomes C, Georgas K, Sullivan T, Verzijl HT, Oley CA, Little M, De Jonghe P, Kwon JM, Kremer H, Dixon MJ, Timmerman V, Yamada T, Koopman P. Hargrave M, et al. Among authors: oley ca. Hum Genet. 2000 Apr;106(4):432-9. doi: 10.1007/s004390000266. Hum Genet. 2000. PMID: 10830911

7

A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.

Crolla JA, Cawdery JE, Oley CA, Young ID, Gray J, Fantes J, van Heyningen V. Crolla JA, et al. Among authors: oley ca. J Med Genet. 1997 Mar;34(3):207-12. doi: 10.1136/jmg.34.3.207. J Med Genet. 1997. PMID: 9132491 Free PMC article.

8

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.

Wilson LC, Leverton K, Oude Luttikhuis ME, Oley CA, Flint J, Wolstenholme J, Duckett DP, Barrow MA, Leonard JV, Read AP, et al. Wilson LC, et al. Among authors: oley ca. Am J Hum Genet. 1995 Feb;56(2):400-7. Am J Hum Genet. 1995. PMID: 7847374 Free PMC article.

9

Evidence for locus heterogeneity in autosomal dominant torsion dystonia.

Ahmad F, Davis MB, Waddy HM, Oley CA, Marsden CD, Harding AE. Ahmad F, et al. Among authors: oley ca. Genomics. 1993 Jan;15(1):9-12. doi: 10.1006/geno.1993.1003. Genomics. 1993. PMID: 8432555

10

Basal cell carcinomas, coarse sparse hair, and milia.

Oley CA, Sharpe H, Chenevix-Trench G. Oley CA, et al. Am J Med Genet. 1992 Jul 15;43(5):799-804. doi: 10.1002/ajmg.1320430509. Am J Med Genet. 1992. PMID: 1642265 No abstract available.

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

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

13 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

13 results

Results by year