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Results: 1 to 20 of 304

Related Citations for PubMed (Select 10090899)

1.

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3.

Cabot A, Rozet JM, Gerber S, Perrault I, Ducroq D, Smahi A, Souied E, Munnich A, Kaplan J.

Am J Hum Genet. 1999 Apr;64(4):1141-6.

2.

Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).

Kerrison JB, Giorda R, Lenart TD, Drack AV, Maumenee IH.

Ophthalmic Genet. 2001 Dec;22(4):241-8.

PMID:
11803490
3.

Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN).

Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC.

Ophthalmic Genet. 2000 Dec;21(4):227-33.

PMID:
11135493
4.

A novel X-linked dominant condition: X-linked congenital isolated ptosis.

McMullan TF, Collins AR, Tyers AG, Robinson DO.

Am J Hum Genet. 2000 Apr;66(4):1455-60. Epub 2000 Mar 14.

5.

[Mapping of a pedigree with congenital nystagmus].

Liu ZR, Zhang BR, Ding MP, Xia K, Hu ZM, Deng H, Xia JH.

Yi Chuan. 2004 Jul;26(4):437-40. Chinese.

PMID:
15640035
6.

A gene for autosomal dominant congenital nystagmus localizes to 6p12.

Kerrison JB, Arnould VJ, Barmada MM, Koenekoop RK, Schmeckpeper BJ, Maumenee IH.

Genomics. 1996 May 1;33(3):523-6.

PMID:
8661013
7.

Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomaly.

Mellott ML, Brown J Jr, Fingert JH, Taylor CM, Keech RV, Sheffield VC, Stone EM.

Arch Ophthalmol. 1999 Dec;117(12):1630-3.

PMID:
10604668
8.

A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

Assink JJ, Tijmes NT, ten Brink JB, Oostra RJ, Riemslag FC, de Jong PT, Bergen AA.

Am J Hum Genet. 1997 Oct;61(4):934-9.

9.

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.

J Clin Invest. 1993 Jun;91(6):2351-7.

10.

Congenital motor nystagmus linked to Xq26-q27.

Kerrison JB, Vagefi MR, Barmada MM, Maumenee IH.

Am J Hum Genet. 1999 Feb;64(2):600-7.

11.

Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.

Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM.

J Med Genet. 2003 Jan;40(1):37-41.

12.

A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

Morlé L, Bozon M, Zech JC, Alloisio N, Raas-Rothschild A, Philippe C, Lambert JC, Godet J, Plauchu H, Edery P.

Am J Hum Genet. 2000 Dec;67(6):1592-7. Epub 2000 Oct 13.

13.

Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?

Ng D, Hadley DW, Tifft CJ, Biesecker LG.

Am J Med Genet. 2002 Jul 15;110(4):308-14.

PMID:
12116202
14.

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Bleeker-Wagemakers LM, Friedrich U, Gal A, Wienker TF, Warburg M, Ropers HH.

Hum Genet. 1985;71(3):211-4.

PMID:
2998969
15.

Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter.

Zhang W, Amir R, Stockton DW, Van Den Veyver IB, Bacino CA, Zoghbi HY.

Am J Hum Genet. 2000 Apr;66(4):1461-4. Epub 2000 Mar 17.

16.

Genetic mapping of a novel X-linked recessive colobomatous microphthalmia.

Lehman DM, Sponsel WE, Stratton RF, Mensah J, Macdonald JC, Johnson-Pais TL, Coon H, Reveles XT, Cody JD, Leach RJ.

Am J Med Genet. 2001 Jun 15;101(2):114-9.

PMID:
11391653
17.

Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family.

Zhang B, Xia K, Ding M, Liang D, Liu Z, Pan Q, Hu Z, Wu LQ, Cai F, Xia J.

Hum Genet. 2005 Jan;116(1-2):128-31. Epub 2004 Oct 23.

PMID:
15517395
18.

A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.

Deqaqi SC, N'Guessan M, Forner J, Sbiti A, Beldjord C, Chelly J, Sefiani A, Des Portes V.

Ann Genet. 1998;41(1):11-6.

PMID:
9599645
19.

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.

Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM.

Hum Genet. 1989 Mar;81(4):315-8.

PMID:
2564836
20.

Autosomal dominant congenital nystagmus is not linked to 6p12, 7p11, and 15q11 in a German family.

Hoffmann S, Becker A, Hoerle S, Metz A, Oertel WH, Sommer N, Hemmer B.

Am J Ophthalmol. 2004 Sep;138(3):439-43.

PMID:
15364228
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