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Search Results - LAROCHE-RAYNAUD, C
Search Results - LAROCHE-RAYNAUD, C
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Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation
by
POIRIER, K
,
ABRIOL, J
,
SOUVILLE, I
,
LAROCHE-RAYNAUD, C
,
BELDJORD, C
,
GILBERT, B
,
CHELLY, J
,
BIENVENU, T
Published in
Human genetics
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The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care
by
de Antonio, M
,
Dogan, C
,
Eymard, B
,
Puymirat, J
,
Mathieu, J
,
Gagnon, C
,
Attarian, S
,
Aube-Nathier, Ac
,
Audic, F
,
Bach, N
,
Barnerias, C
,
Bedat-Millet, Al
,
Behin, A
,
Bellance, R
,
Ben Yaou, R
,
Bombard, V
,
Bouhour, F
,
Boutte, C
,
Boyer, F
,
Cances, C
,
Chabrol, B
,
Chanson, Jb
,
Chapon, F
,
Chasseriau, R
,
Cintas, P
,
Cobo, Am
,
Colombert, V
,
Cruz, Mc
,
Cuisset, Jm
,
Deschamps, R
,
Desguerre, I
,
Durigneux, J
,
Duval, F
,
Espil, C
,
Fafin, C
,
Feasson, L
,
Fradin, M
,
Furby, A
,
Goldenberg, A
,
Grotto, S
,
Ghorab, K
,
Guyant-Marechal, L
,
Heron, D
,
Isapof, A
,
Jacquin-Piques, A
,
Journel, H
,
Laforet, P
,
Lagrue, E
,
Laroche-Raynaud, C
,
Laugel, V
,
Lebeau, F
,
Magot, A
,
Manel, V
,
Mayer, M
,
Mercier, S
,
Menard, D
,
Michaud, M
,
Minot, Mc
,
Morales, Rj
,
Nadaj-Pakleza, A
,
Noury, Jb
,
Pasquier, L
,
Pellieux, S
,
Pereon, Y
,
Perrier, J
,
Peudenier, S
,
Preudhomme, M
,
Pouget, J
,
Quijano-Roy, S
,
Ragot-Mandry, S
,
Richelme, C
,
Rivier, F
,
Sabouraud, P
,
Sacconi, S
,
Salort-Campana, E
,
Sarret, C
,
Schaeffer, S
,
Sole, G
,
Stojkovic, T
,
Taithe, F
,
Testard, H
,
Tiffereau, V
,
Urtizberea, A
,
Vanhulle, C
,
Vial, C
,
Walther-Louvier, U
,
Zagnoli, F
,
Hamroun, D
,
Bassez, G
Published in
Orphanet journal of rare diseases
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Targeted therapy in patients with PIK3CA-related overgrowth syndrome
by
Venot, Quitterie
,
Blanc, Thomas
,
Rabia, Smail Hadj
,
Berteloot, Laureline
,
Ladraa, Sophia
,
Duong, Jean-Paul
,
Blanc, Estelle
,
Johnson, Simon C
,
Hoguin, Clément
,
Boccara, Olivia
,
Sarnacki, Sabine
,
Boddaert, Nathalie
,
Pannier, Stephanie
,
Martinez, Frank
,
Magassa, Sato
,
Yamaguchi, Junna
,
Knebelmann, Bertrand
,
Merville, Pierre
,
Grenier, Nicolas
,
Joly, Dominique
,
Cormier-Daire, Valérie
,
Michot, Caroline
,
Bole-Feysot, Christine
,
Picard, Arnaud
,
Soupre, Véronique
,
Lyonnet, Stanislas
,
Sadoine, Jeremy
,
Slimani, Lotfi
,
Chaussain, Catherine
,
Laroche-Raynaud, Cécile
,
Guibaud, Laurent
,
Broissand, Christine
,
Amiel, Jeanne
,
Legendre, Christophe
,
Terzi, Fabiola
,
Canaud, Guillaume
Published in
Nature (London)
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Author Correction: Targeted therapy in patients with PIK3CA-related overgrowth syndrome
by
Venot, Quitterie
,
Blanc, Thomas
,
Rabia, Smail Hadj
,
Berteloot, Laureline
,
Ladraa, Sophia
,
Duong, Jean-Paul
,
Blanc, Estelle
,
Johnson, Simon C
,
Hoguin, Clément
,
Boccara, Olivia
,
Sarnacki, Sabine
,
Boddaert, Nathalie
,
Pannier, Stephanie
,
Martinez, Frank
,
Magassa, Sato
,
Yamaguchi, Junna
,
Knebelmann, Bertrand
,
Merville, Pierre
,
Grenier, Nicolas
,
Joly, Dominique
,
Cormier-Daire, Valérie
,
Michot, Caroline
,
Bole-Feysot, Christine
,
Picard, Arnaud
,
Soupre, Véronique
,
Lyonnet, Stanislas
,
Sadoine, Jeremy
,
Slimani, Lotfi
,
Chaussain, Catherine
,
Laroche-Raynaud, Cécile
,
Guibaud, Laurent
,
Broissand, Christine
,
Amiel, Jeanne
,
Legendre, Christophe
,
Terzi, Fabiola
,
Canaud, Guillaume
Published in
Nature (London)
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Microduplication 1p36.3 chez un enfant de 2ans avec retard global de développement
by
Marquet, Valentine
,
Bourthoumieux, Sylvie
,
Laroche-Raynaud, Cécile
,
Yardin, Catherine
Published in
Morphologie
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Microduplication 1p36.3 chez un enfant de 2 ans avec retard global de développement
by
Marquet, Valentine
,
Bourthoumieux, Sylvie
,
Laroche-Raynaud, Cécile
,
Yardin, Catherine
Published in
Morphologie
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