Authors:
Chavanas, S
Bodemer, C
Rochat, A
Hamel-Teillac, D
Ali, M
Irvine, AD
Bonafe, JL
Wilkinson, J
Taieb, A
Barrandon, Y
Harper, JI
de Prost, Y
Hovnanian, A
Citation: S. Chavanas et al., Mutations in SPINK5, encoding a serine protease inhibitor, cause Nethertonsyndrome, NAT GENET, 25(2), 2000, pp. 141-142
Authors:
Lefevre, P
Rochat, A
Bodemer, C
Vabres, P
Barrandon, Y
de Prost, Y
Garner, C
Hovnanian, A
Citation: P. Lefevre et al., Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusionof 10 genes including the hairless gene by mutation analysis, EUR J HUM G, 8(4), 2000, pp. 273-279
Citation: A. Rochat, Unpublished texts (Introduction to 'Gens du bord de l'eau' and 'Vigneron, moi aussi' by Charles-Ferdinand Ramuz), EUR-REV LIT, 78(853), 2000, pp. 31-32
Authors:
Rugg, EL
Rachet-Prehu, MO
Rochat, A
Barrandon, Y
Goossens, M
Lane, EB
Hovnanian, A
Citation: El. Rugg et al., Donor splice site mutation in keratin 5 causes in-frame removal of 22 amino acids of H1 and 1A rod domains in Dowling-Meara epidermolysis bullosa simplex, EUR J HUM G, 7(3), 1999, pp. 293-300