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Results: 1 to 20 of 1081

Similar articles for PubMed (Select 19218600)

1.

Replication of the recessive STBMS1 locus but with dominant inheritance.

Rice A, Nsengimana J, Simmons IG, Toomes C, Hoole J, Willoughby CE, Cassidy F, Williams GA, George ND, Sheridan E, Young TL, Hunter TI, Barrett BT, Elliott DB, Bishop DT, Inglehearn CF.

Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3210-7. doi: 10.1167/iovs.07-1631. Epub 2009 Feb 14.

PMID:
19218600
2.

Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus.

Shaaban S, Matsuo T, Fujiwara H, Itoshima E, Furuse T, Hasebe S, Zhang Q, Ott J, Ohtsuki H.

Invest Ophthalmol Vis Sci. 2009 Feb;50(2):654-61. doi: 10.1167/iovs.08-2437. Epub 2008 Sep 29.

PMID:
18824738
3.

[Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion].

Xiong G, Deng FY, Xiao B, Yang XS, Ning JC, Wu ZG, Wang K, Deng HW.

Zhonghua Er Ke Za Zhi. 2004 Jun;42(6):424-8. Chinese.

PMID:
15265426
4.

Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.

Mineharu Y, Inoue K, Inoue S, Yamada S, Nozaki K, Hashimoto N, Koizumi A.

Stroke. 2007 Apr;38(4):1174-8. Epub 2007 Feb 22.

5.

CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.

Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.

Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2458-65.

PMID:
11581183
6.

Linkage analysis of high myopia susceptibility locus in 26 families.

Paget S, Julia S, Vitezica ZG, Soler V, Malecaze F, Calvas P.

Mol Vis. 2008;14:2566-74. Epub 2008 Dec 30.

7.

A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q.

Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen KR, Rosso A, Donald JA, Adams LJ, Schofield PR.

Mol Psychiatry. 2001 Jul;6(4):396-403.

8.

Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?

Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.

Neurology. 2008 Feb 26;70(9):686-94. Epub 2007 Nov 21.

PMID:
18032746
9.

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, Hewitt AW, Latimer P, Craig JE.

Hum Genet. 2008 Nov;124(4):379-86. doi: 10.1007/s00439-008-0555-z. Epub 2008 Sep 5.

PMID:
18795334
10.

Genome-wide search for strabismus susceptibility loci.

Fujiwara H, Matsuo T, Sato M, Yamane T, Kitada M, Hasebe S, Ohtsuki H.

Acta Med Okayama. 2003 Jun;57(3):109-16.

11.

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.

Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.

Mov Disord. 2006 Jan;21(1):28-33.

PMID:
16124010
12.

New Alzheimer's disease locus on chromosome 8.

Giedraitis V, Hedlund M, Skoglund L, Blom E, Ingvast S, Brundin R, Lannfelt L, Glaser A.

J Med Genet. 2006 Dec;43(12):931-5. Epub 2006 Jul 6.

13.

Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles.

Traboulsi EI, Lee BA, Mousawi A, Khamis AR, Engle EC.

Am J Ophthalmol. 2000 May;129(5):658-62.

PMID:
10844060
14.

Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders.

Camp NJ, Lowry MR, Richards RL, Plenk AM, Carter C, Hensel CH, Abkevich V, Skolnick MH, Shattuck D, Rowe KG, Hughes DC, Cannon-Albright LA.

Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):85-93.

PMID:
15806581
15.

The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.

McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA.

Br J Ophthalmol. 2005 Jul;89(7):831-4.

16.

An autosomal genomic screen for autism.

Collaborative Linkage Study of Autism.

Am J Med Genet. 2001 Dec 8;105(8):609-15.

PMID:
11811142
17.

Juvenile glaucoma linked to GLCIA in a Panamanian family.

Lichter PR, Richards JE, Boehnke M, Othman M, Cameron BD, Stringham HM, Downs CA, Lewis SB, Boyd BF.

Trans Am Ophthalmol Soc. 1996;94:335-46; discussion 347-51.

18.

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
19.

Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome.

Khan AO, Shinwari J, Al Sharif L, Khalil D, Al-Gehedan S, Tassan NA.

Mol Vis. 2011;17:1997-2002. Epub 2011 Jul 20.

20.

[The human major histocompatibility complex region is not a major susceptibility locus for Graves disease among the Hans in north of China].

Jin Y, Hu F, Teng W, Ben S, Zhang J, Xiong X, Huang W.

Zhonghua Yi Xue Za Zhi. 2002 Sep 25;82(18):1242-4. Chinese.

PMID:
12425802
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