Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
Sanlaville, D, Etchevers, H C, Gonzales, M, Martinovic, J, Clément-Ziza, M, Delezoide, A-L, Aubry, M-C, Pelet, A, Chemouny, S, Cruaud, C, Audollent, S, Esculpavit, C, Goudefroye, G, Ozilou, C, Fredouille, C, Joye, N, Morichon-Delvallez, N, Dumez, Y, Weissenbach, J, Munnich, A, Amiel, J, Encha-Razavi, F, Lyonnet, S, Vekemans, M, Attié-Bitach, T
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects
Lepagnol-Bestel, A-M, Maussion, G, Boda, B, Cardona, A, Iwayama, Y, Delezoide, A-L, Moalic, J-M, Muller, D, Dean, B, Yoshikawa, T, Gorwood, P, Buxbaum, J D, Ramoz, N, Simonneau, M
Published in Molecular psychiatry (01.04.2008)
Published in Molecular psychiatry (01.04.2008)
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Contribution of Diffusion-Weighted Imaging in the Evaluation of Diffuse White Matter Ischemic Lesions in Fetuses: Correlations with Fetopathologic Findings
Guimiot, F, Garel, C, Fallet-Bianco, C, Menez, F, Khung-Savatovsky, S, Oury, J.-F, Sebag, G, Delezoide, A.-L
Published in American journal of neuroradiology : AJNR (01.01.2008)
Published in American journal of neuroradiology : AJNR (01.01.2008)
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Fetal phenotypes in otopalatodigital spectrum disorders
Naudion, S., Moutton, S., Coupry, I., Sole, G., Deforges, J., Guerineau, E., Hubert, C., Deves, S., Pilliod, J., Rooryck, C., Abel, C., Le Breton, F., Collardeau-Frachon, S., Cordier, M.P., Delezoide, A.L., Goldenberg, A., Loget, P., Melki, J., Odent, S., Patrier, S., Verloes, A., Viot, G., Blesson, S., Bessières, B., Lacombe, D., Arveiler, B., Goizet, C., Fergelot, P.
Published in Clinical genetics (01.03.2016)
Published in Clinical genetics (01.03.2016)
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Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis
Guimiot, F., Dupont, C., Fuentes‐Duarte, A., Aboura, A., Bazin, A., Khung‐Savatovsky, S., Tillous‐Borde, I., Delezoide, A.‐L., Azancot, A.
Published in American journal of medical genetics. Part A (01.01.2013)
Published in American journal of medical genetics. Part A (01.01.2013)
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Ultrasound detection of hyaloid artery in the third trimester of pregnancy: a pathological finding
Spaggiari, E., Vuillard, E., Baumann, C., Dupont, C., Belarbi, N., Oury, J.‐F., Delezoide, A.‐L., Guimiot, F.
Published in Ultrasound in obstetrics & gynecology (01.04.2012)
Published in Ultrasound in obstetrics & gynecology (01.04.2012)
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P25.09: Posterior urethral valves and vesicoureteral reflux: can prenatal ultrasonography distinguish between these two conditions in male fetuses?
Chitrit, Y., Bourdon, M., Peycelon, M., Grapin‐Dagorno, C., Korb, D., Joinau‐Zoulovits, F., Vuillard, E., Paye‐Jaouen, A., Schmitz, T., Belarbi, N., Delezoide, A., El Ghoneimi, A., Sibony, O., Oury, J.
Published in Ultrasound in obstetrics & gynecology (01.09.2016)
Published in Ultrasound in obstetrics & gynecology (01.09.2016)
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Foetal serum but not urinary β2-microglobulin correlates with histological injury to the kidney
Luton, D., Delezoide, A.L., Leguy, M.C., Gobeaux, C., Vuillard, E., Grangé, G., Guibourdenche, J.
Published in Clinical biochemistry (01.10.2013)
Published in Clinical biochemistry (01.10.2013)
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Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly
Odent, S., Attié-Bitach, T., Blayau, M., Mathieu, M., Augé, J., Delezoïde, A.L., Le Gall, J.Y., Le Marec, B., Munnich, A., David, V., Vekemans, M.
Published in Human molecular genetics (01.09.1999)
Published in Human molecular genetics (01.09.1999)
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Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature
Levaillant, J. M., Moeglin, D., Zouiten, K., Bucourt, M., Burglen, L., Soupre, V., Baumann, C., Jaquemont, M. L., Touraine, R., Picard, A., Vuillard, E., Belarbi, N., Oury, J. F., Verloes, A., Vazquez, M. P., Labrune, P., Delezoide, A. L., Gérard-Blanluet, M.
Published in Prenatal diagnosis (01.02.2009)
Published in Prenatal diagnosis (01.02.2009)
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The Distribution of SMN Protein Complex in Human Fetal Tissues and Its Alteration in Spinal Muscular Atrophy
Burlet, P., Huber, C., Bertrandy, S., Ludosky, M. A., Zwaenepoel, I., Clermont, O., Roume, J., Delezoide, A. L., Cartaud, J., Munnich, A., Lefebvre, S.
Published in Human molecular genetics (01.11.1998)
Published in Human molecular genetics (01.11.1998)
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Missense FGFR3 Mutations Create Cysteine Residues in Thanatophoric Dwarfism Type I (TD1)
Rousseau, F., El Ghouzzi, V., Delezoide, A. L., Legeai-Mallet, L., Le Merrer, M., Munnich, A., Bonaventure, J.
Published in Human molecular genetics (01.04.1996)
Published in Human molecular genetics (01.04.1996)
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Twin-to-Twin Transfusion Syndrome : Role of the Fetal Renin-Angiotensin System
Mahieu-Caputo, Dominique, Dommergues, Marc, Delezoide, Anne-Lise, Lacoste, Mireille, Cai, Yi, Narcy, Francoise, Jolly, Dominique, Gonzales, Marie, Dumez, Yves, Gubler, Marie-Claire
Published in The American journal of pathology (01.02.2000)
Published in The American journal of pathology (01.02.2000)
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Comparison between magnetic resonance imaging and fetopathology in the evaluation of fetal posterior fossa non‐cystic abnormalities
Tilea, B., Delezoide, A. L., Khung‐Savatovski, S., Guimiot, F., Vuillard, E., Oury, J. F., Garel, C.
Published in Ultrasound in obstetrics & gynecology (01.06.2007)
Published in Ultrasound in obstetrics & gynecology (01.06.2007)
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Correlation between low FAT1 expression and early affected muscle in FSHD
Mariot, V, Roche, S, Hourdé, C, Portilho, D, Sacconi, S, Puppo, F, Duguez, S, Rameau, P, Caruso, N, Delezoide, A, Desnuelle, C, Bessières, B, Collardeau, S, Feasson, L, Maisonobe, T, Magdinier, F, Helmbacher, F, Butler-Browne, G, Mouly, V, Dumonceaux, J
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families
Bouchet, C., Vuillaumier-Barrot, S., Gonzales, M., Boukari, S., Bizec, C. Le, Fallet, C., Delezoide, A.-L., Moirot, H., Laquerriere, A., Encha-Razavi, F., Durand, G., Seta, N.
Published in Molecular genetics and metabolism (2007)
Published in Molecular genetics and metabolism (2007)
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Prenatal rupture of a left ventricular diverticulum: a case report and review of the literature
Bernasconi, A., Delezoide, A. L., Menez, F., Vuillard, E., Oury, J. F., Azancot, A.
Published in Prenatal diagnosis (01.07.2004)
Published in Prenatal diagnosis (01.07.2004)
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C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome
Rachidi, M., Lopes, C., Delezoide, A.-L., Delabar, J.M.
Published in Cytogenetic and genome research (01.01.2006)
Published in Cytogenetic and genome research (01.01.2006)
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