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Items: 8

1.

Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse.

Stottmann RW, Bjork BC, Doyle JB, Beier DR.

Genesis. 2010 May;48(5):303-8. doi: 10.1002/dvg.20618.

2.

Toward an orofacial gene regulatory network.

Kousa YA, Schutte BC.

Dev Dyn. 2016 Mar;245(3):220-32. doi: 10.1002/dvdy.24341. Epub 2015 Sep 17. Review.

3.

IRF6-Related Disorders.

Schutte BC, Saal HM, Goudy S, Leslie E.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mefford HC, Stephens K, Amemiya A, Ledbetter N, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2003 Oct 30 [updated 2014 Jul 3].

4.

Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: review of the literature.

Salahshourifar I, Wan Sulaiman WA, Halim AS, Zilfalil BA.

Eur J Med Genet. 2012 Jun;55(6-7):389-93. doi: 10.1016/j.ejmg.2012.02.006. Epub 2012 Mar 3. Review.

PMID:
22440537
5.

Genetics of syndromic and nonsyndromic cleft lip and palate.

Stuppia L, Capogreco M, Marzo G, La Rovere D, Antonucci I, Gatta V, Palka G, Mortellaro C, Tetè S.

J Craniofac Surg. 2011 Sep;22(5):1722-6. doi: 10.1097/SCS.0b013e31822e5e4d. Review.

PMID:
21959420
6.

A familial case of popliteal pterygium syndrome.

Bertelè G, Mercanti M, Gangini GN, Carletti V.

Minerva Stomatol. 2008 Jun;57(6):309-22. Review. English, Italian.

PMID:
18617879
7.

Grainyhead-like Transcription Factors in Craniofacial Development.

Carpinelli MR, de Vries ME, Jane SM, Dworkin S.

J Dent Res. 2017 Oct;96(11):1200-1209. doi: 10.1177/0022034517719264. Epub 2017 Jul 11. Review.

PMID:
28697314
8.

Genetic Factors in Selected Complex Congenital Malformations with Cleft Defect.

Wójcicki P, Koźlik MJ, Wójcicka K.

Adv Clin Exp Med. 2016 Sep-Oct;25(5):977-987. doi: 10.17219/acem/61911. Review.

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