Συγγραφείς:
Manolakos, E.
Sifakis, S.
Sotiriou, S.
Peitsidis, P.
Eleftheriades, M.
Mersinias, V.
Liehr, T.
Thomaidis, L.
Kitsos, G.
Papoulidis, I.
Petersen, M.B.
Orru, S.
Λέξεις-κλειδιά:
genomic DNA, adult; amnion cell; article; case report; chorion villus sampling; chromosome 1q; chromosome analysis; chromosome deletion; chromosome duplication; chromosome inversion; chromosome rearrangement; copy number variation; Down syndrome; embryo; female; fetus; fetus echography; fetus hydrops; fluorescence in situ hybridization; genetic counseling; genetic risk; human; human cell; karyotype; medical literature; nuchal translucency measurement; partial trisomy; partial trisomy 1q; polymerase chain reaction; pregnancy termination; prenatal screening; priority journal, Adult; Chromosome Deletion; Chromosome Duplication; Chromosome Inversion; Chromosomes, Human, Pair 1; Cytogenetic Analysis; Female; Fetal Diseases; Fetus; Humans; Hydrops Fetalis; Nuchal Translucency Measurement; Pregnancy; Prenatal Diagnosis; Trisomy