Non-Invasive Detection of a De Novo Frameshift Variant of STAG2 in a Female Fetus: Escape Genes Influence the Manifestation of X-Linked Diseases in Females von Provenzano, Aldesia, La Barbera, Andrea, Lai, Francesco, Perra, Andrea, Farina, Antonio, Cariati, Ettore, Zuffardi, Orsetta, Giglio, Sabrina

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Metatropic dysplasia in third trimester of pregnancy and a novel causative variant in the TRPV4 gene von Bargiacchi, Sara, Della Monica, Matteo, Biagiotti, Roberto, Andreucci, Elena, Ciabattoni, Serena, Poggi, Paolo, Di Maurizio, Marco, Defilippi, Claudio, Cariati, Ettore, Giglio, Sabrina, MD, PhD

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Prenatal twisting of minimally conjoined omphalopagus twins von Maiandi, Erika A., Biagiotti, Roberto, Garbini, Francesca, Cariati, Ettore

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Prenatal diagnosis of X‐linked adrenoleukodystrophy associated with isolated pericardial effusion von Traficante, Giovanna, Biagiotti, Roberto, Andreucci, Elena, Di Tommaso, Mariarosaria, Provenzano, Aldesia, Cariati, Ettore, Giglio, Sabrina

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First trimester screening for Down's syndrome using maternal serum PAPP‐A and free β=hCG in combination with fetal nuchal translucency thickness von Biagiotti, Roberto, Brizn, Laura, Periti, Enrico, D'Agata, Albertino, VanZi, Ermanno, Cariati, Ettore

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Maternal serum screening for trisomy 18 in the first trimester of pregnancy von Biagiotti, Roberto, Cariati, Ettore, Brizzi, Laura, Cappelli, Gino, D'Agata, Alberino

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Humerus and femur length in fetuses with down syndrome von Biagiotti, Roberto, Periti, Enrico, Cariati, Ettore

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Maternal serum screening for Down's syndrome in the first trimester of pregnancy von Biagiotti, Roberto, Cariati, Ettore, Brizzi, Laura, D'Agata, Alberino

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Prenatal diagnosis of X-linked adrenoleukodystrophy associated with isolated pericardial effusion von Traficante, Giovanna, Biagiotti, Roberto, Andreucci, Elena, Di Tommaso, Mariarosaria, Provenzano, Aldesia, Cariati, Ettore, Giglio, Sabrina

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Prenatal twisting of minimally conjoined omphalopagus twins von Maiandi, Erika A, Biagiotti, Roberto, Garbini, Francesca, Cariati, Ettore

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Prenatal Detection of Congenital Renal Malformations by Fetal Ultrasonographic Examination: An Analysis of 709,030 Births in 12 European Countries von Wiesel, A., Queisser-Luft, A., Clementi, M., Bianca, S., Stoll, C.

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Turner syndrome: Evaluation of prenatal diagnosis in 19 European registries von Baena, Neus, De Vigan, C., Cariati, E., Clementi, M., Stoll, C., Caballín, M.R., Guitart, M.

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Prenatal ultrasonographic detection of gastrointestinal obstruction: results from 18 European congenital anomaly registries von Haeusler, Martin C. H., Berghold, Andrea, Stoll, Claude, Barisic, Ingeborg, Clementi, Maurizio

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Prenatal detection of rare chromosomal autosomal abnormalities in Europe von Baena, N., De Vigan, C., Cariati, E., Clementi, M., Stoll, C., Caballin, M.R., Guitart, M.

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Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across Europe von Stoll, C., Tenconi, R., Clementi, M.

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