Login
|
New Account
AAAAAA
ITA
ENG
Results:
1-4
|
Results: 4
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
Authors:
Finegold, DN Kimak, MA Lawrence, EC Levinson, KL Cherniske, EM Pober, BR Dunlap, JW Ferrell, RE
Citation:
Dn. Finegold et al., Truncating mutations in FOXC2 cause multiple lymphedema syndromes, HUM MOL GEN, 10(11), 2001, pp. 1185-1189
VEGFR3 gene structure, regulatory region, and sequence polymorphisms
Authors:
Iljin, K Karkkainen, MJ Lawrence, EC Kimak, MA Uutela, M Taipale, J Pajusola, K Alhonen, L Halmekyto, M Finegold, DN Ferrell, RE Alitalo, K
Citation:
K. Iljin et al., VEGFR3 gene structure, regulatory region, and sequence polymorphisms, FASEB J, 15(6), 2001, pp. 1028-1036
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
Authors:
Karkkainen, MJ Ferrell, RE Lawrence, EC Kimak, MA Levinson, KL McTigue, MA Alitalo, K Finegold, DN
Citation:
Mj. Karkkainen et al., Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema, NAT GENET, 25(2), 2000, pp. 153-159
Hereditary lymphedema: evidence for linkage and genetic heterogeneity
Authors:
Ferrell, RE Levinson, KL Esman, JH Kimak, MA Lawrence, EC Barmada, MM Finegold, DN
Citation:
Re. Ferrell et al., Hereditary lymphedema: evidence for linkage and genetic heterogeneity, HUM MOL GEN, 7(13), 1998, pp. 2073-2078
Risultati:
1-4
|