Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases
Author(s) -
Sezin Yakut,
Zafer Çetin,
Mehmet Şımşek,
Ibrahim Inanc Mendicioglu,
Havva Serap Toru,
Sibel Berker Karaüzüm,
Güven Lüleci
Publication year - 2014
Publication title -
turkish journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.305
H-Index - 14
eISSN - 1309-5730
pISSN - 1018-5615
DOI - 10.5146/tjpath.2014.01280
Subject(s) - chromosomal translocation , prenatal diagnosis , amniocentesis , chorionic villus sampling , genetic counseling , supernumerary , fluorescence in situ hybridization , karyotype , abnormality , biology , autopsy , pathology , genetics , obstetrics , medicine , chromosome , fetus , pregnancy , anatomy , gene , psychiatry
Objective: The aim of this study was presentation of the ultrasonographic findings and perinatal autopsy of cases with rare chromosomal abnormalities.
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