Outcome of first‐trimester chorionic villus sampling for genetic investigation in multiple pregnancy von Brambati, B., Tului, L., Guercilena, S., Alberti, E.

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Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samples von Pertl, Barbara, Kopp, Susanne, Kroisel, Peter M, Tului, Lucia, Brambati, Bruno, Adinolfi, Matteo

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Low maternal serum levels of pregnancy associated plasma protein A (PAPP‐A) in the first trimester in association with abnormal fetal karyotype von Brambati, B., Macintosh, M. C. M., Teisner, B., Maguiness, S., Shrimanker, K., Lanzani, A., Bonacchi, I., Tului, L., Chard, T., Grudzinskas, J. G.

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First‐trimester Down's syndrome screening using nuchal translucency: a prospective study in patients undergoing chorionic villus sampling von Brambati, B., Cislaghi, C., Tului, L., Alberti, E., Amidani, M., Colombo, U., Zuliani, G.

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First trimester concentrations of pregnancy associated plasma protein A and placental protein 14 in Down's syndrome von Wald, N., Stone, R., Cuckle, H. S., Grudzinskas, J. G., Barkai, G., Brambati, B., Teisner, B., Fuhrmann, W.

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Chorionic villus sampling safety von KULIEV, A, JACKSON, L, FROSTER, U, BRAMBATI, B, SIMPSON, J. L, VERLINSKY, Y, SMIDT-JENSEN, S, ZAKUT, H

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First-trimester fetal reduction to a singleton infant or twins: Outcome in relation to the final number and karyotyping before reduction by transabdominal chorionic villus sampling von Brambati, Bruno, Tului, Lucia, Camurri, Lamberto, Guercilena, Stefano

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Chorionic villus sampling and amniocentesis von Brambati, Bruno, Tului, Lucia

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Management of multiple pregnancy: fetal reduction and prenatal diagnosis von Brambati, B, Tului, L

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Serum PAPP-A and free β-hCG are first-trimester screening markers for down syndrome von Brambati, B., Tului, L., Bonacchi, I., Shrimanker, K., Suzuki, Y., Grudzinskas, J. G.

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Chorionic villus sampling von Brambati, B

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The Euro-Team Early Pregnancy (ETEP) protocol for recurrent miscarriage von Berry, C.W., Brambati, B., Eskes, T.K.A.B., Exalto, N., Fox, H., Geraedts, J.P.M., Gerhard, I., Gomes, F.Gonzales, Grudzinskas, J.G., Hustin, J., Jouppila, P., Lindblom, B.K.A., Mantoni, M., Montenegro, N., Fernandes, F.Nogales, O'Rahilly, R., Pedersen, J.F., Peters, P.W.J., Regan, L., Rushton, D.I., van Straaten, H.W.M., Tarlatzis, B.C., Wells, M.

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Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions von Guerneri, Silvana, Bettio, Daniela, Simoni, G., Brambati, B., Lanzani, A., Fraccaro, M.

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Improvement in outcomes of multifetal pregnancy reduction with increased experience von Evans, Mark I., Berkowitz, Richard L., Wapner, Ronald J., Carpenter, Robert J., Goldberg, James D., Ayoub, Melissa A., Horenstein, Janet, Dommergues, Marc, Brambati, Bruno, Nicolaides, Kypros H., Holzgreve, Wolfgang, Timor-Tritsch, Ilan E.

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Selective termination for structural, chromosomal, and mendelian anomalies: International experience von Evans, Mark I., Goldberg, James D., Horenstein, Janet, Wapner, Ronald J., Ayoub, Melissa A., Stone, Joanne, Lipitz, Shlomo, Achiron, Rueven, Holzgreve, Wolfgang, Brambati, Bruno, Johnson, Anthony, Johnson, Mark P., Shalhoub, Alex, Berkowitz, Richard L.

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Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagn... von Galluzzi, G, Deidda, G, Cacurri, S, Colantoni, L, Piazzo, N, Vigneti, E, Ricci, E, Servidei, S, Merico, B, Pachı̀, A, Brambati, B, Mangiola, F, Tonali, P, Felicetti, L

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Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy von Simoni, G, Brambati, B, Danesino, C, Rossella, F, Terzoli, G L, Ferrari, M, Fraccaro, M

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Ethical guidance on human embryonic and fetal tissue transplantation: a European overview von de, Wert G, Berghmans, R L, Boer, G J, Andersen, S, Brambati, B, Carvalho, A S, Dierickx, K, Elliston, S, Nunez, P, Osswald, W, Vicari, M

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Prenatal diagnosis of genetic diseases: Special Issue: Millennium Issue: Historical Reviews in Obstetrics and Gynecology von BRAMBATI, B

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Prenatal diagnosis of genetic diseases von Brambati, Bruno

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