Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency von Hyon, C, Mansour-Hendili, L, Chantot-Bastaraud, S, Donadille, B, Kerlan, V, Dodé, C, Jonard, S, Delemer, B, Gompel, A, Reznik, Y, Touraine, P, Siffroi, J. P, Christin-Maitre, S

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Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation von Frapsauce, C., Ravel, C., Legendre, M., Sibony, M., Mandelbaum, J., Donadille, B., Achermann, J.C., Siffroi, J.-P., Christin-Maitre, S.

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Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly von Lavillaureix, A., Heide, S., Chantot‐Bastaraud, S., Marey, I., Keren, B., Grigorescu, R., Jouannic, J.M., Gelot, A., Whalen, S., Héron, D., Siffroi, J.P.

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Identification of transcripts by macroarrays, RT–PCR and in situ hybridization in human ejaculate spermatozoa von Dadoune, J.P., Pawlak, A., Alfonsi, M.F., Siffroi, J.P.

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Added value of buccal cell FISH analysis in the diagnosis and management of Turner syndrome von Graff, A., Donadille, B., Morel, H., Villy, M. C., Bourcigaux, N., Vatier, C., Borgel, A., Khodawardi, A., Siffroi, J. P., Christin-Maitre, S.

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Causes rares d’anomalies de l’empreinte parentale entraînant un retard de croissance à début intra-utérin (RCIU) von Pham, A, Chantot-Bastaraud, S., Dr, Siffroi, J.-P., Pr, Mitanchez, D., Pr, Netchine, I., Pr

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Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men von Gekas, J., Thepot, F., Turleau, C., Siffroi, J.P., Dadoune, J.P., Briault, S., Rio, M., Bourouillou, G., Carré-Pigeon, F., Wasels, R., Benzacken, B., Association des Cytogeneticiensde Langue Francaise, The

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Mutations in the protamine 1 gene associated with male infertility von Ravel, C., Chantot-Bastaraud, S., El Houate, B., Berthaut, I., Verstraete, L., De Larouziere, V., Lourenço, D., Dumaine, A., Antoine, J.M., Mandelbaum, J., Siffroi, J.P., McElreavey, K.

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O01 Obtention d’adipocytes beiges humains fonctionnels in vitro et in vivo à partir de cellules souches à pluripotence induite von Guénantin, A.-C, Briand, N, Capel, E, Stillitano, F, Jeziorowska, D, Morichon, R, Siffroi, J.-P, Fève, B, Capeau, J, Hulot, J.-S, Vigouroux, C

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Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study von Aknin-Seifer, I.E., Touraine, R.L., Lejeune, H., Jimenez, C., Chouteau, J., Siffroi, J.P., McElreavey, K., Bienvenu, T., Patrat, C., Levy, R.

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Underlying karyotype abnormalities in IVF/ICSI patients von Chantot-Bastaraud, S, Ravel, C, Siffroi, JP

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Quality assessment of induced spermatogenesis in hypogonadotrophic hypogonadic men treated with gonadotrophins von Krabchi, K, Berthaut, I, Chantot-Bastaraud, S, Ravel, C, Chabbert-Buffet, N, de Larouzière, V, Bouchard, P, Mandelbaum, J, Siffroi, J.-P, Christin-Maitre, S

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Stratégies reproductives et transmission des gènes: grâce aux femmes et malgré les hommes ? von Siffroi, J.-P.

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Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26 von Ravel, C., El Houate, B., Chantot, S., Lourenço, D., Dumaine, A., Rouba, H., Bandyopadahyay, A., Radhakrishna, U., Das, B., Sengupta, S., Mandelbaum, J., Siffroi, J.P., McElreavey, K.

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Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinoma von Bourcigaux, N, Rubino, C, Berthaud, I, Toubert, M E, Donadille, B, Leenhardt, L, Petrot-Keller, I, Brailly-Tabard, S, Fromigué, J, de Vathaire, F, Simon, T, Siffroi, J P, Schlumberger, M, Bouchard, P, Christin-Maitre, S

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Sperm-FISH analysis in a pericentric chromosome 1 inversion, 46,XY,inv(1)(p22q42), associated with infertility von Chantot-Bastaraud, S., Ravel, C., Berthaut, I., McElreavey, K., Bouchard, P., Mandelbaum, J., Siffroi, J.P.

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A high frequency of Y chromosome deletions in males with nonidiopathic infertility von KRAUSZ, C, QUINTANA-MURCI, L, TAAR, J. P, TAR, A, JEANDIDIER, E, PLESSIS, G, BOURGERON, T, DADOUNE, J.-P, FELLOUS, M, MCELREAVEY, K, BARBAUX, S, SIFFROI, J.-P, ROUBA, H, DELAFONTAINE, D, SOULEYREAU-THERVILLE, N, ARVIS, G, ANTOINE, J. M, ERDEI, E

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Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysis von Marlin, S., Ducou Le Pointe, H., Le Merrer, M., Portnoi, M.F., Chantot, S., Jonard, L., Mantel‐Guiochon, A., Siffroi, J.P., Garabedian, E.N., Denoyelle, F.

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Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses von Vialard, F, Ottolenghi, C, Gonzales, M, Choiset, A, Girard, S, Siffroi, J P, McElreavey, K, Vibert-Guigue, C, Sebaoun, M, Joyé, N, Portnoï, M F, Jaubert, F, Fellous, M

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Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism von Krausz, Csilla, Quintana-Murci, Lluis, Fellous, Marc, Siffroi, Jean-Pierre, McElreavey, Ken

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