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
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
Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13
Authors:
Vats, A Nayak, A Ellis, D Randhawa, PS Finegold, DN Levinson, KL Ferrell, RE
Citation:
A. Vats et al., Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13, KIDNEY INT, 57(3), 2000, pp. 875-881
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
|