Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?

por Miny, Peter, Wenzel, Friedel, Tercanli, Sevgi, Filges, Isabel
Publicado 2013

Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?

por Hahn, Sinuhe, Lapaire, Olav, Tercanli, Sevgi, Kolla, Varaprasad, Hösli, Irene
Publicado 2011

Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly

por Meier, Nicole, Bruder, Elisabeth, Miny, Peter, Tercanli, Sevgi, Filges, Isabel
Publicado 2020

Quantitative Proteomics Analysis of Maternal Plasma in Down Syndrome Pregnancies Using Isobaric Tagging Reagent (iTRAQ)

por Kolla, Varaprasad, Jenö, Paul, Moes, Suzette, Tercanli, Sevgi, Lapaire, Olav, Choolani, Mahesh, Hahn, Sinuhe
Publicado 2010

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies

por Filges, Isabel, Kang, Anjeung, Klug, Vanessa, Wenzel, Friedel, Heinimann, Karl, Tercanli, Sevgi, Miny, Peter
Publicado 2012

Potential markers of preeclampsia – a review

por Grill, Simon, Rusterholz, Corinne, Zanetti-Dällenbach, Rosanna, Tercanli, Sevgi, Holzgreve, Wolfgang, Hahn, Sinuhe, Lapaire, Olav
Publicado 2009

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

por Meier, Nicole, Bruder, Elisabeth, Lapaire, Olav, Hoesli, Irene, Kang, Anjeung, Hench, Jürgen, Hoeller, Sylvia, De Geyter, Julie, Miny, Peter, Heinimann, Karl, Chaoui, Rabih, Tercanli, Sevgi, Filges, Isabel
Publicado 2019