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Items: 6

1.

Keratoconus in 18 pairs of twins.

Tuft SJ, Hassan H, George S, Frazer DG, Willoughby CE, Liskova P.

Acta Ophthalmol. 2012 Sep;90(6):e482-6. doi: 10.1111/j.1755-3768.2012.02448.x. Epub 2012 Jun 8.

2.

Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.

Schulz AC, Bartels E, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Heydweiller A, Bachour H, Schumacher J, Bartmann P, Nöthen MM, Reutter H.

Birth Defects Res A Clin Mol Teratol. 2012 Mar;94(3):182-6. doi: 10.1002/bdra.22879. Epub 2012 Jan 30. Review.

PMID:
22287212
3.

Cleft-twin sets in Finland 1948-1987.

Nordström RE, Laatikainen T, Juvonen TO, Ranta RE.

Cleft Palate Craniofac J. 1996 Jul;33(4):340-7. Review.

PMID:
8827393
4.
5.

Differential genetic etiology of reading difficulties as a function of IQ: an update.

Wadsworth SJ, Olson RK, DeFries JC.

Behav Genet. 2010 Nov;40(6):751-8. doi: 10.1007/s10519-010-9349-x. Epub 2010 Mar 24. Review.

6.

What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration.

Ketelaar ME, Hofstra EM, Hayden MR.

Clin Genet. 2012 Apr;81(4):325-33. doi: 10.1111/j.1399-0004.2011.01795.x. Epub 2011 Nov 12. Review.

PMID:
21981075
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