Pallister-killian Syndrome: Rare Phenotypic Features and Variable Karyotypes
نویسنده
چکیده
1 Institut für Humangenetik und Anthropologie, Kollegien gasse 10, D-07743 Jena, Germany 2 Zentrum für Pränataldiagnostik, Kurfürstendamm 199, D-10719 Berlin, Germany 3 Vinca Institute of Nuclear Sciences, POB 522, in cooperation with Institute of Laboratory Medicine Aqualab, 11.000 Belgrade, Serbia 4 Republican Medical Center “Mother and child”, Scientific department, Orlovskaya str, 66, bl.8, Minsk 220053, Republic of Belarus *Corresponding Author: Dr. Thomas Liehr, Institut für Humangenetik, Postfach D-07740 Jena, Germany; Tel: +49-3641-935533; Fax. ++49-3641-935582; e-mail: [email protected] Liehr T1,*, Wegner R-D2, Stumm M2, Joksić G3, Polityko A4, Kosyakova N1, Ewers E1, Reich D1, Wagner R1, Weise A1
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تاریخ انتشار 2009