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Items: 1 to 20 of 99

1.

Dominantly inherited cutaneous small-vessel lymphocytic vasculitis maps to chromosome 6q26-q27.

Sellick GS, Coleman RJ, Webb EL, Chow J, Bevan S, Rosbotham JL, Houlston RS.

Hum Genet. 2005 Oct;118(1):82-6. Epub 2005 Oct 28.

PMID:
16133183
2.
3.

Cloning and mapping of human chromosome 6q26-q27 deleted in B-cell non-Hodgkin lymphoma and multiple tumor types.

Hauptschein RS, Gamberi B, Rao PH, Frigeri F, Scotto L, Venkatraj VS, Gaidano G, Rutner T, Edwards YH, Chaganti RS, Dalla-Favera R.

Genomics. 1998 Jun 1;50(2):170-86.

PMID:
9653644
4.

A novel locus for autosomal dominant cone and cone-rod dystrophies maps to the 6p gene cluster of retinal dystrophies.

Castori M, Valente EM, Clementi M, Tormene AP, Brancati F, Caputo V, Dallapiccola B.

Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3539-44.

PMID:
16186331
5.

A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

Zhang Q, Guo X, Xiao X, Jia X, Li S, Hejtmancik JF.

Mol Vis. 2005 Jul 22;11:554-60.

6.

Mapping a new familial thyroid epithelial neoplasia susceptibility locus to chromosome 8p23.1-p22 by high-density single-nucleotide polymorphism genome-wide linkage analysis.

Cavaco BM, Batista PF, Sobrinho LG, Leite V.

J Clin Endocrinol Metab. 2008 Nov;93(11):4426-30. doi: 10.1210/jc.2008-0449. Epub 2008 Sep 2.

PMID:
18765515
7.

[A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].

Yu ZQ, Li YB, Huang CX, Chu RY, Hu DN, Shen ZH, Huang W.

Zhonghua Yan Ke Za Zhi. 2007 Mar;43(3):233-8. Chinese.

PMID:
17605906
8.

Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.

Malik S, Grzeschik KH.

Hum Genet. 2008 Mar;123(2):197-205. doi: 10.1007/s00439-007-0458-4. Epub 2008 Jan 10.

PMID:
18193458
9.

The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype.

Patel H, Hart PE, Warner TT, Houlston RS, Patton MA, Jeffery S, Crosby AH.

Am J Hum Genet. 2001 Jul;69(1):209-15. Epub 2001 May 25.

10.

A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2-q12.

Yang Y, Guo J, Liu Z, Tang S, Li N, Yang M, Pang Q, Fan F, Bu J, Yuan ST, Xiao X, Chen Y, Zhao K.

Hum Genet. 2006 Aug;120(1):144-7. Epub 2006 Jun 15.

PMID:
16775710
11.

Evidence for clinical and genetic heterogeneity in hereditary benign telangiectasia.

Molho-Pessach V, Agha Z, Libster D, Lerer I, Burger A, Jaber S, Abeliovich D, Zlotogorski A.

J Am Acad Dermatol. 2007 Nov;57(5):814-8. Epub 2007 Jul 20.

PMID:
17658662
12.

A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.

Tlili A, Männikkö M, Charfedine I, Lahmar I, Benzina Z, Ben Amor M, Driss N, Ala-Kokko L, Drira M, Masmoudi S, Ayadi H.

Hum Hered. 2005;60(3):123-8. Epub 2005 Oct 18.

PMID:
16244493
13.

A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension.

Disse-Nicodème S, Achard JM, Desitter I, Houot AM, Fournier A, Corvol P, Jeunemaitre X.

Am J Hum Genet. 2000 Aug;67(2):302-10. Epub 2000 Jun 22.

14.

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.

Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N, O'Donovan MC, Owen MJ.

Mol Psychiatry. 2010 Nov;15(11):1101-11. doi: 10.1038/mp.2009.96. Epub 2009 Sep 29.

PMID:
19786960
15.

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.

Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L.

Neurology. 2009 Jun 2;72(22):1893-8. doi: 10.1212/WNL.0b013e3181a6086c. Epub 2009 Apr 8.

PMID:
19357379
16.

Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.

Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y.

J Am Soc Nephrol. 2007 Aug;18(8):2408-15. Epub 2007 Jul 18.

17.

High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.

Liskova P, Gwilliam R, Filipec M, Jirsova K, Reinstein Merjava S, Deloukas P, Webb TR, Bhattacharya SS, Ebenezer ND, Morris AG, Hardcastle AJ.

PLoS One. 2012;7(9):e45495. doi: 10.1371/journal.pone.0045495. Epub 2012 Sep 25.

18.

Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.

Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML.

Hum Mol Genet. 1994 Sep;3(9):1583-7.

PMID:
7833915
19.

Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus.

Jordan SA, del Rio T, Soriano N, Garcia-Sandoval B, Kenna P, Ayuso C, Benitez J, Humphries P.

Hum Mol Genet. 1992 Sep;1(6):411-5.

PMID:
1301915
20.

Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.

Lee-Kirsch MA, Gong M, Schulz H, Rüschendorf F, Stein A, Pfeiffer C, Ballarini A, Gahr M, Hubner N, Linné M.

Am J Hum Genet. 2006 Oct;79(4):731-7. Epub 2006 Aug 17.

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