Format
Sort by

Send to

Choose Destination

Selected items

Items: 3

1.

Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.

Shovlin CL, Hughes JM, Scott J, Seidman CE, Seidman JG.

Am J Hum Genet. 1997 Jul;61(1):68-79.

2.

Characterization of 17 novel endoglin mutations associated with hereditary hemorrhagic telangiectasia.

Cymerman U, Vera S, Karabegovic A, Abdalla S, Letarte M.

Hum Mutat. 2003 May;21(5):482-92.

PMID:
12673790
3.

Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients.

Lesca G, Burnichon N, Raux G, Tosi M, Pinson S, Marion MJ, Babin E, Gilbert-Dussardier B, Rivière S, Goizet C, Faivre L, Plauchu H, Frébourg T, Calender A, Giraud S; French Rendu-Osler Network.

Hum Mutat. 2006 Jun;27(6):598.

PMID:
16705692

Supplemental Content

Support Center