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Items: 5

1.

GJC2 missense mutations cause human lymphedema.

Ferrell RE, Baty CJ, Kimak MA, Karlsson JM, Lawrence EC, Franke-Snyder M, Meriney SD, Feingold E, Finegold DN.

Am J Hum Genet. 2010 Jun 11;86(6):943-8. doi: 10.1016/j.ajhg.2010.04.010. Epub 2010 May 27.

2.

Connexins in lymphatic vessel physiology and disease.

Meens MJ, Sabine A, Petrova TV, Kwak BR.

FEBS Lett. 2014 Apr 17;588(8):1271-7. doi: 10.1016/j.febslet.2014.01.011. Epub 2014 Jan 20. Review.

3.

Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review.

Dellinger MT, Thome K, Bernas MJ, Erickson RP, Witte MH.

Lymphology. 2008 Sep;41(3):98-102. Review.

PMID:
19013876
4.

Genetics of lymphatic anomalies.

Brouillard P, Boon L, Vikkula M.

J Clin Invest. 2014 Mar;124(3):898-904. doi: 10.1172/JCI71614. Epub 2014 Mar 3. Review.

5.

Research perspectives in inherited lymphatic disease.

Ferrell RE.

Ann N Y Acad Sci. 2002 Dec;979:39-51; discussion 76-9. Review.

PMID:
12543715

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