Authors:
Sztriha, L
Frossard, P
Hofstra, RMW
Verlind, E
Nork, M
Citation: L. Sztriha et al., Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus, J CHILD NEU, 15(4), 2000, pp. 239-243
Authors:
Lestringant, GG
Bener, A
Frossard, P
Townsend, A
Citation: Gg. Lestringant et al., Association of Acanthosis nigricans with risk of diabetes mellitus and hormonal disturbances in females, INT J GYN O, 71(3), 2000, pp. 267-269
Authors:
Romey, MC
Guittard, C
Chazalette, JP
Frossard, P
Dawson, KP
Patton, MA
Casals, T
Bazarbachi, T
Girodon, E
Rault, G
Bozon, D
Seguret, F
Demaille, J
Claustres, M
Citation: Mc. Romey et al., Complex allele [-102T > A+S549R(T > G)] is associated with milder forms ofcystic fibrosis than allele S549R[T > G) alone, HUM GENET, 105(1-2), 1999, pp. 145-150
Authors:
Mardy, S
Miura, Y
Endo, F
Matsuda, I
Sztriha, L
Frossard, P
Moosa, A
Ismail, EAR
Macaya, A
Andria, G
Toscano, E
Gibson, W
Graham, GE
Indo, Y
Citation: S. Mardy et al., Congenital insensitivity to pain with anhidrosis: Novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor, AM J HU GEN, 64(6), 1999, pp. 1570-1579