First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)
Martin-Denavit, T., Attia-Sobol, J., Theuil, J., Abel-Lablanche, K., Boggio, D., Teyssier, M., Till, M., Champion, F., Vitrey, D., Plauchu, H.
Published in Prenatal diagnosis (01.06.2002)
Published in Prenatal diagnosis (01.06.2002)
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Usefulness of procalcitonin in neonates at risk for infection
Martin-Denavit, T, Monneret, G, Labaune, J M, Isaac, C, Bienvenu, F, Putet, G, Bienvenu, J
Published in Clinical chemistry (Baltimore, Md.) (01.03.1999)
Published in Clinical chemistry (Baltimore, Md.) (01.03.1999)
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Ectodermal abnormalities associated with methimazole intrauterine exposure
Martin-Denavit, T, Edery, P, Plauchu, H, Attia-Sobol, J, Raudrant, D, Aurand, J M, Thomas, L
Published in American journal of medical genetics (02.10.2000)
Published in American journal of medical genetics (02.10.2000)
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Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines
Dreux, Sophie, Rosenblatt, Jonathan, Benachi, Alexandra, Voirin‐Mathieu, Etienne, Muller, Françoise, Boitte, F., Denis, M. C., Lorenter, P., Jouval, M., Sitruk, B., Suybeng, V., Herbreteau, S., Treyssac, F., Gras, V., Guiot, J., Savarit, D., Blouin, P., Zanusso, M., Clément, P., Brossaud, J., Fischer, I., Moineau, M. P., Kerspern, H., Andlauer, P., Gaeremynck, E., Berchiche, S., Barba, F., Lebrun, C., Terrier, N., Kemeny, S., Delevallée, C., Marceau, G., Gehrke, C., Lemaire, S., Ménégaut, L., Lefaure, G., Petit, V., Gauchez‐Quenin, A. S., Pavili, L., Chevallier‐Helas, F., Artur, F., Sigogneau, P., Groussin, H., Renom, G., Lepers, S., Chianéa, T., Veyrat, B., Le Querler, L., Martin‐Denavit, T., Sault, C., Galland, A., Cheillan, D., Brechard, M. P., Yerokine, P., Levy‐Mozziconacci, A., Toga, C., Sainte‐Rose, M., Wasels, R., Aubertin, D., Rahil, H., Roucaute, T., Boulle, N., Solassol, J., Minery, M., Baillet, C., Dauch, P., Chevillon, I., Masson, D., Rotella, C. M., Barguil, Y., Duhin, M., Got, L., Lachgar, M., Druart, L., Ramirez, J. M., Lacroix, I., Brethome, B., Cassuto, G., Cohen‐Bacrie, M., Ternaux, F., Beaujard, M. P., Annette‐Reisch, M., Bounaud, M. P., Nowak, E., Dossot, J. M., Odaert, H., Quillard Murain, M., Descombes, G., Belot, G., Tisseur, B., Gouneaud, J., Louzier, C., Tosetti, F., Romain, S., Handwerk, L., Molignier, R., De Mas, P., Le Van, M., Estepa, B., Tang, K.
Published in Prenatal diagnosis (01.07.2024)
Published in Prenatal diagnosis (01.07.2024)
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Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3)
Sanlaville, Damien, Vialard, François, Thépot, François, Vue-Droy, Luce, Ardalan, Azarnouche, Nizard, Patrice, Corré, Alain, Devauchelle, Bernard, Martin-Denavit, Tanguy, Nouchy, Marc, Malan, Valérie, Taillemite, Jean-Louis, Portnoï, Marie-France
Published in American journal of medical genetics. Part A (30.07.2004)
Published in American journal of medical genetics. Part A (30.07.2004)
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A new case of a severe clinical phenotype of the cat-eye syndrome
Denavit, T Martin, Malan, V, Grillon, C, Sanlaville, D, Ardalan, A, Jacquemont, M L, Burglen, L, Taillemite, J L, Portnoi, M F
Published in Genetic counseling (2004)
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Published in Genetic counseling (2004)
Journal Article
First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)
Martin-Denavit, T, Attia-Sobol, J, Theuil, J, Abel-Lablanche, K, Boggio, D, Teyssier, M, Till, M, Champion, F, Vitrey, D, Plauchu, H
Published in Prenatal diagnosis (01.06.2002)
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Published in Prenatal diagnosis (01.06.2002)
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