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Results: 1 to 20 of 78

1.

Sequence variant in the laminin gamma1 (LAMC1) gene associated with familial pelvic organ prolapse.

Nikolova G, Lee H, Berkovitz S, Nelson S, Sinsheimer J, Vilain E, Rodríguez LV.

Hum Genet. 2007 Feb;120(6):847-56. Epub 2006 Oct 5.

PMID:
17021862
[PubMed - indexed for MEDLINE]
2.

Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse?

Chen C, Hill LD, Schubert CM, Strauss JF 3rd, Matthews CA.

Am J Obstet Gynecol. 2010 May;202(5):505.e1-5. doi: 10.1016/j.ajog.2010.01.014. Epub 2010 Mar 12.

PMID:
20223449
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.

Guleria K, Sperling K, Singh D, Varon R, Singh JR, Vanita V.

Mol Vis. 2007 Sep 11;13:1657-65.

PMID:
17893674
[PubMed - indexed for MEDLINE]
Free Article
4.

Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse.

Wu JM, Visco AG, Grass EA, Craig DM, Fulton RG, Haynes C, Amundsen CL, Shah SH.

Am J Obstet Gynecol. 2012 May;206(5):447.e1-6. doi: 10.1016/j.ajog.2012.01.033. Epub 2012 Jan 31.

PMID:
22342894
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Familial brain arteriovenous malformation maps to 5p13-q14, 15q11-q13 or 18p11: linkage analysis with clipped fingernail DNA on high-density SNP array.

Oikawa M, Kuniba H, Kondoh T, Kinoshita A, Nagayasu T, Niikawa N, Yoshiura K.

Eur J Med Genet. 2010 Sep-Oct;53(5):244-9. doi: 10.1016/j.ejmg.2010.06.007. Epub 2010 Jun 22.

PMID:
20601259
[PubMed - indexed for MEDLINE]
6.

Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.

Nürnberg G, Jacobi FK, Broghammer M, Becker C, Blin N, Nürnberg P, Stephani U, Pusch CM.

Int J Mol Med. 2008 Apr;21(4):429-38.

PMID:
18360688
[PubMed - indexed for MEDLINE]
7.

Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: a SNP array-based linkage analysis of 38 families.

Suh I, Filetti S, Vriens MR, Guerrero MA, Tumino S, Wong M, Shen WT, Kebebew E, Duh QY, Clark OH.

Surgery. 2009 Dec;146(6):1073-80. doi: 10.1016/j.surg.2009.09.012.

PMID:
19958934
[PubMed - indexed for MEDLINE]
8.

SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K.

Hum Mol Genet. 2007 Oct 15;16(20):2482-93. Epub 2007 Jul 25.

PMID:
17656375
[PubMed - indexed for MEDLINE]
Free Article
9.

Differential gene expression in pubococcygeus muscle from patients with pelvic organ prolapse.

Visco AG, Yuan L.

Am J Obstet Gynecol. 2003 Jul;189(1):102-12.

PMID:
12861146
[PubMed - indexed for MEDLINE]
10.

Evaluation of the ARMD1 locus on 1q25-31 in patients with age-related maculopathy: genetic variation in laminin genes and in exon 104 of HEMICENTIN-1.

Hayashi M, Merriam JE, Klaver CC, Zernant J, Bergen AA, Smith RT, Chang S, Merriam JC, Allikmets R.

Ophthalmic Genet. 2004 Jun;25(2):111-9.

PMID:
15370542
[PubMed - indexed for MEDLINE]
11.

Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.

Gurnett CA, Alaee F, Kruse LM, Desruisseau DM, Hecht JT, Wise CA, Bowcock AM, Dobbs MB.

Am J Hum Genet. 2008 Nov;83(5):616-22. doi: 10.1016/j.ajhg.2008.10.004. Epub 2008 Oct 23.

PMID:
18950742
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

The EPHA2 gene is associated with cataracts linked to chromosome 1p.

Shiels A, Bennett TM, Knopf HL, Maraini G, Li A, Jiao X, Hejtmancik JF.

Mol Vis. 2008;14:2042-55. Epub 2008 Nov 12.

PMID:
19005574
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.

Mol Psychiatry. 2007 Apr;12(4):376-84. Epub 2006 Dec 19.

PMID:
17179998
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

Identification of IRF6 gene variants in three families with Van der Woude syndrome.

Tan EC, Lim EC, Yap SH, Lee ST, Cheng J, Por YC, Yeow V.

Int J Mol Med. 2008 Jun;21(6):747-51.

PMID:
18506368
[PubMed - indexed for MEDLINE]
16.

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.

Hmani-Aifa M, Ben Salem S, Benzina Z, Bouassida W, Messaoud R, Turki K, Khairallah M, Rebaï A, Fakhfekh F, Söderkvist P, Ayadi H.

Hum Genet. 2009 Oct;126(4):575-87. doi: 10.1007/s00439-009-0688-8. Epub 2009 Jun 14.

PMID:
19526372
[PubMed - indexed for MEDLINE]
17.

Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the beta-subunit of transducin with digenic disease.

Gao YQ, Danciger M, Ozgul RK, Gribanova Y, Jacobson S, Farber DB.

Mol Vis. 2007 Feb 28;13:287-92.

PMID:
17356515
[PubMed - indexed for MEDLINE]
Free PMC Article
18.
19.

A genome-wide association study of sporadic ALS in a homogenous Irish population.

Cronin S, Berger S, Ding J, Schymick JC, Washecka N, Hernandez DG, Greenway MJ, Bradley DG, Traynor BJ, Hardiman O.

Hum Mol Genet. 2008 Mar 1;17(5):768-74. Epub 2007 Dec 5.

PMID:
18057069
[PubMed - indexed for MEDLINE]
Free Article
20.

Polymorphism of the gene encoding alpha-1 chain of collagen type I and a risk of pelvic organ prolapse--a preliminary study.

Skorupski P, Miotła P, Jankiewicz K, Rechberger T.

Ginekol Pol. 2007 Nov;78(11):852-5.

PMID:
18306915
[PubMed - indexed for MEDLINE]

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