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Results:
1-10
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Results: 10
Authors:
Brown, LY
Odent, S
David, V
Blayau, M
Dubourg, C
Apacik, C
Delgado, MA
Ha, BD
Reynolds, JF
Sommer, A
Wieczorek, D
Brown, SA
Muenke, M
Citation: Ly. Brown et al., Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination, HUM MOL GEN, 10(8), 2001, pp. 791-796
Authors:
Dussaulx-Garin, L
Blayau, M
Pagenault, M
Le Berre-Heresbach, N
Raoul, JL
Campion, JP
David, V
Bretagne, JF
Citation: L. Dussaulx-garin et al., A new mutation of E-cadherin gene in familial gastric linitis plastica cancer with extra-digestive dissemination, EUR J GASTR, 13(6), 2001, pp. 711-715
Authors:
Amaral, MD
Pacheco, P
Beck, S
Farinha, CM
Penque, D
Nogueira, P
Barreto, C
Lopes, B
Casals, T
Dapena, J
Gartner, S
Vasquez, C
Perez-Frias, J
Olveira, C
Cabanas, R
Estivill, X
Tzetis, M
Kanavakis, E
Doudounakis, S
Dork, T
Tummler, B
Girodon-Boulandet, E
Cazeneuve, C
Goossens, M
Blayau, M
Verlingue, C
Vieira, I
Ferec, C
Claustres, M
des Georges, M
Clavel, C
Birembaut, P
Hubert, D
Bienvenu, T
Adoun, M
Chomel, JC
De Boeck, K
Cuppens, H
Lavinha, J
Citation: Md. Amaral et al., Cystic fibrosis patients with the 3272-26A > G splicing mutation have milder disease than F508del homozygotes: a large European study, J MED GENET, 38(11), 2001, pp. 777-782
Authors:
Jezequel, P
Dubourg, C
Le Lannou, D
Odent, S
Le Gall, JY
Blayau, M
Le Treut, A
David, V
Citation: P. Jezequel et al., Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations, MOL HUM REP, 6(12), 2000, pp. 1063-1067
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence ofthe vas deferens in France
Authors:
Claustres, M
Guittard, C
Bozon, D
Chevalier, F
Verlingue, C
Ferec, C
Girodon, E
Cazeneuve, C
Bienvenu, T
Lalau, G
Dumur, V
Feldmann, D
Bieth, E
Blayau, M
Clavel, C
Creveaux, I
Malinge, MC
Monnier, N
Malzac, P
Mittre, H
Chomel, JC
Bonnefont, JP
Iron, A
Chery, M
Des Georges, M
Citation: M. Claustres et al., Spectrum of CFTR mutations in cystic fibrosis and in congenital absence ofthe vas deferens in France, HUM MUTAT, 16(2), 2000, pp. 143-156
Authors:
Pasquier, L
Dubourg, C
Blayau, M
Lazaro, L
Le Marec, B
David, V
Odent, S
Citation: L. Pasquier et al., A new mutation in the six-domain of SIX3 gene causes holoprosencephaly, EUR J HUM G, 8(10), 2000, pp. 797-800
Authors:
Odent, S
Attie-Bitach, T
Blayau, M
Mathieu, M
Auge, J
Delezoide, AL
Le Gall, JY
Le Marec, B
Munnich, A
David, V
Vekemans, M
Citation: S. Odent et al., Expression of the Sonic hedgehog (SHH) gene during early human developmentand phenotypic expression of new mutations causing holoprosencephaly, HUM MOL GEN, 8(9), 1999, pp. 1683-1689
Authors:
Odent, S
Attie-Bitach, T
Blayau, M
Mathieu, M
Auge, J
Delezoide, AL
Le Gall, JY
Le Marec, B
Munnich, A
David, V
Vekemans, M
Citation: S. Odent et al., Expression of the Sonic hedgehog (SHH) gene during early human developmentand phenotypic expression of new mutations causing holoprosencephaly (vol 8, pg 1683, 1999), HUM MOL GEN, 8(12), 1999, pp. 2335-2335
Authors:
Des Georges, M
Guittard, C
Bozon, D
Chevalier, F
Verlingue, C
Ferec, C
Girodon, E
Cazeneuve, C
Bienvenu, T
Lalau, G
Dumur, V
Feldmann, D
Bieth, E
Blayau, M
Clavel, C
Creveaux, I
Malinge, MC
Monnier, N
Malzac, P
Mittre, H
Bonnefont, JP
Iron, A
Chomel, JC
Chery, M
Claustres, M
Citation: M. Des Georges et al., Molecular basis of cystic fibrosis in France: more than 300 different mutations and 506 genotypes are involved, M S-MED SCI, 14(12), 1998, pp. 1413-1421
Authors:
Blayau, M
Odent, S
Dubourg, C
David, V
Citation: M. Blayau et al., FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variant, HUM GENET, 103(5), 1998, pp. 626-627
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1-10
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