Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
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Published in Neuromuscular disorders : NMD (01.10.2015)
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Ramanah, R., Martin, A., Guigue, V., Arbez‐Gindre, F., Piard, J., Terrosi, P., Alanio, E., Favre, R., Gaillard, D., Riethmuller, D.
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Published in Ultrasound in obstetrics & gynecology (01.12.2012)
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Michel, M.E, Alanio, E, Bois, E, Gavillon, N, Graesslin, O
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Published in European journal of obstetrics & gynecology and reproductive biology (01.03.2010)
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Ducellier, G, Moussy, P, Sahmoune, L, Bonneau, S, Alanio, E, Bory, J-P
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Published in Gynécologie, obstétrique & fertilité (01.09.2016)
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Published in Annales de chirurgie plastique et esthétique (01.10.2016)
Published in Annales de chirurgie plastique et esthétique (01.10.2016)
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G.O.4 - Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
Ravenscroft, G., Nolent, F., Rajagopalan, S., Meireles, A., Paavola, K., Gaillard, D., Alanio, E., Buckland, M., Arbuckle, S., Krivanek, M., Maluenda, J., Pannell, S., Gooding, R., Ong, R., Allcock, R., Kok, F., Talbot, W., Melki, J., Laing, N.
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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L’ombilic chez l’enfant
Jayyosi, L., Boudaoud, N., Okiemy, O., Correia, N., Alanio-Detton, E., Bory, J.P., Liné, A., Poli-Merol, M.L., Mazouz Dorval, S., Francois, C.
Published in Annales de chirurgie plastique et esthétique (01.10.2016)
Published in Annales de chirurgie plastique et esthétique (01.10.2016)
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Bardet-Biedl syndrome - antenatal presentation of 45 fetuses with biallelic pathogenic variants in known BBS genes
Mary, L, Chennen, K, Stoetzel, C, Antin, M, Leuvrey, A S, Nourisson, E, Alanio-Detton, E, Antal, M C, Attie-Bitach, T, Bouvagnet, P, Bouvier, R, Buenerd, A, Clémenson, A, Devisme, L, Gasser, B, Gilbert-Dussardier, B, Guimiot, F, Khau Van Kien, P, Leroy, B, Loget, P, Martinovic, J, Pelluard, F, Perez, M J, Petit, F, Pinson, L, Rooryck, C, Poch, O, Dollfus, H, Schaefer, E, Muller, J
Published in Clinical genetics (07.01.2019)
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Published in Clinical genetics (07.01.2019)
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