Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 29

1.

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.

Bruder CE, Piotrowski A, Gijsbers AA, Andersson R, Erickson S, Diaz de Ståhl T, Menzel U, Sandgren J, von Tell D, Poplawski A, Crowley M, Crasto C, Partridge EC, Tiwari H, Allison DB, Komorowski J, van Ommen GJ, Boomsma DI, Pedersen NL, den Dunnen JT, Wirdefeldt K, Dumanski JP.

Am J Hum Genet. 2008 Mar;82(3):763-71. doi: 10.1016/j.ajhg.2007.12.011. Epub 2008 Feb 14.

2.

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.

Osoegawa K, Vessere GM, Utami KH, Mansilla MA, Johnson MK, Riley BM, L'Heureux J, Pfundt R, Staaf J, van der Vliet WA, Lidral AC, Schoenmakers EF, Borg A, Schutte BC, Lammer EJ, Murray JC, de Jong PJ.

J Med Genet. 2008 Feb;45(2):81-6. Epub 2007 Sep 14.

3.

Impaired FGF signaling contributes to cleft lip and palate.

Riley BM, Mansilla MA, Ma J, Daack-Hirsch S, Maher BS, Raffensperger LM, Russo ET, Vieira AR, Dodé C, Mohammadi M, Marazita ML, Murray JC.

Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4512-7. Epub 2007 Mar 6.

4.

Whole genome genotyping technologies on the BeadArray platform.

Steemers FJ, Gunderson KL.

Biotechnol J. 2007 Jan;2(1):41-9.

PMID:
17225249
5.

A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate.

Watanabe A, Akita S, Tin NT, Natsume N, Nakano Y, Niikawa N, Uchiyama T, Yoshiura K.

Cleft Palate Craniofac J. 2006 May;43(3):310-6.

PMID:
16681403
6.

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes.

Lupski JR, Stankiewicz P.

PLoS Genet. 2005 Dec;1(6):e49. Review.

7.

Structural variation in the human genome.

Feuk L, Carson AR, Scherer SW.

Nat Rev Genet. 2006 Feb;7(2):85-97. Review.

PMID:
16418744
8.

Comparative genomic hybridization.

Pinkel D, Albertson DG.

Annu Rev Genomics Hum Genet. 2005;6:331-54. Review.

PMID:
16124865
9.

Orofacial clefting: recent insights into a complex trait.

Jugessur A, Murray JC.

Curr Opin Genet Dev. 2005 Jun;15(3):270-8. Review.

10.

Lesch-Nyhan disease in a female with a clinically normal monozygotic twin.

De Gregorio L, Jinnah HA, Harris JC, Nyhan WL, Schretlen DJ, Trombley LM, O'Neill JP.

Mol Genet Metab. 2005 May;85(1):70-7. Epub 2005 Feb 17.

PMID:
15862283
11.

Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits.

Mansilla MA, Kimani J, Mitchell LE, Christensen K, Boomsma DI, Daack-Hirsch S, Nepomucena B, Wyszynski DF, Felix TM, Martin NG, Murray JC.

Twin Res Hum Genet. 2005 Feb;8(1):39-46.

PMID:
15836809
12.

Phenotypic differences in genetically identical organisms: the epigenetic perspective.

Wong AH, Gottesman II, Petronis A.

Hum Mol Genet. 2005 Apr 15;14 Spec No 1:R11-8. Review.

13.

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

Matsuzaki H, Dong S, Loi H, Di X, Liu G, Hubbell E, Law J, Berntsen T, Chadha M, Hui H, Yang G, Kennedy GC, Webster TA, Cawley S, Walsh PS, Jones KW, Fodor SP, Mei R.

Nat Methods. 2004 Nov;1(2):109-11.

PMID:
15782172
14.

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu YE, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC.

N Engl J Med. 2004 Aug 19;351(8):769-80.

16.

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.

Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC.

J Med Genet. 2003 Jun;40(6):399-407.

17.

Classical twin studies and beyond.

Boomsma D, Busjahn A, Peltonen L.

Nat Rev Genet. 2002 Nov;3(11):872-82. Review.

PMID:
12415317
18.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC.

Nat Genet. 2002 Oct;32(2):285-9. Epub 2002 Sep 3.

19.

Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling.

Gilbert B, Yardin C, Briault S, Belin V, Lienhardt A, Aubard Y, Battin J, Servaud M, Philippe HJ, Lacombe D.

Prenat Diagn. 2002 Aug;22(8):697-702. Review.

PMID:
12210579
20.

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.

Weksberg R, Shuman C, Caluseriu O, Smith AC, Fei YL, Nishikawa J, Stockley TL, Best L, Chitayat D, Olney A, Ives E, Schneider A, Bestor TH, Li M, Sadowski P, Squire J.

Hum Mol Genet. 2002 May 15;11(11):1317-25.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk