Similar articles for PMID: 9199568

Year	Number of Results
1983	1
1985	4
1986	2
1987	7
1988	7
1989	3
1990	4
1991	4
1992	3
1993	4
1994	7
1995	6
1996	3
1997	6
1998	8
1999	3
2000	9
2001	2
2002	3
2003	1
2004	3
2005	4
2007	1
2008	1
2009	1
2010	2
2013	1
2017	1
2024	0

1

Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.

Bergen AA, Pinckers AJ. Bergen AA, et al. Am J Hum Genet. 1997 Jun;60(6):1468-73. doi: 10.1086/515458. Am J Hum Genet. 1997. PMID: 9199568 Free PMC article.

2

DNA carrier detection in X-linked progressive cone dystrophy.

Bergen AA, Meire F, Schuurman EJ, Delleman JW. Bergen AA, et al. Clin Genet. 1994 May;45(5):236-40. doi: 10.1111/j.1399-0004.1994.tb04148.x. Clin Genet. 1994. PMID: 8076408

3

LOD scores, location scores, and X-linked cone dystrophy.

Inglehearn CF. Inglehearn CF. Am J Hum Genet. 1998 Sep;63(3):900-1. doi: 10.1086/301995. Am J Hum Genet. 1998. PMID: 9718326 Free PMC article. No abstract available.

4

A new genetic locus for X linked progressive cone-rod dystrophy.

Jalkanen R, Demirci FY, Tyynismaa H, Bech-Hansen T, Meindl A, Peippo M, Mäntyjärvi M, Gorin MB, Alitalo T. Jalkanen R, et al. J Med Genet. 2003 Jun;40(6):418-23. doi: 10.1136/jmg.40.6.418. J Med Genet. 2003. PMID: 12807962 Free PMC article.

5

X-linked cone dystrophy.

Verdoorn C, Pinckers A. Verdoorn C, et al. Doc Ophthalmol. 1988 Oct-Nov;70(2-3):195-8. doi: 10.1007/BF00154453. Doc Ophthalmol. 1988. PMID: 3234184

6

A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13.

Balciuniene J, Johansson K, Sandgren O, Wachtmeister L, Holmgren G, Forsman K. Balciuniene J, et al. Genomics. 1995 Nov 20;30(2):281-6. doi: 10.1006/geno.1995.9876. Genomics. 1995. PMID: 8586428

7

X-linked high myopia associated with cone dysfunction.

Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky AG, King RA. Young TL, et al. Arch Ophthalmol. 2004 Jun;122(6):897-908. doi: 10.1001/archopht.122.6.897. Arch Ophthalmol. 2004. PMID: 15197065

8

Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).

Hong HK, Ferrell RE, Gorin MB. Hong HK, et al. Am J Hum Genet. 1994 Dec;55(6):1173-81. Am J Hum Genet. 1994. PMID: 7977377 Free PMC article.

9

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ. Gardner JC, et al. Am J Hum Genet. 2010 Jul 9;87(1):26-39. doi: 10.1016/j.ajhg.2010.05.019. Epub 2010 Jun 24. Am J Hum Genet. 2010. PMID: 20579627 Free PMC article.

10

Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy.

Mäntyjärvi M, Nurmenniemi P, Partanen J, Myöhänen T, Peippo M, Alitalo T. Mäntyjärvi M, et al. Acta Ophthalmol Scand. 2001 Aug;79(4):359-65. doi: 10.1034/j.1600-0420.2001.079004359.x. Acta Ophthalmol Scand. 2001. PMID: 11453854 Free article.

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