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1 Ergebnisse
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The clinical phenotype of Koolen-de Vries syndrome in Turki..:
Yılmaz, Ayşegül
;
Karamık, Gökçen
;
Tüysüz, Beyhan
...
American Journal of Medical Genetics Part A. , 2023
Link:
https://hdl.handle.net/11499/51017
RT Journal T1
The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review
UL https://suche.suub.uni-bremen.de/peid=base-ftpamukkaleuniv:oai:gcris.pau.edu.tr:11499_51017&Exemplar=1&LAN=DE A1 Yılmaz, Ayşegül A1 Karamık, Gökçen A1 Tüysüz, Beyhan A1 Işık, Esra A1 Alanay, Yasemin A1 Çiftçi Sunamak, Evrim A1 Durmusalioglu, Enise Avcı A1 Ozkinay, Ferda A1 Cetin, Gokhan Ozan A1 Ozturk, Nuray A1 Mihci, Ercan PB Wiley YR 2023 K1 17q21 K1 31 microdeletion syndrome K1 KdVS K1 Koolen-de Vries syndrome K1 molecular karyotyping K1 17q21.31 Microdeletion Syndrome K1 Common Inversion K1 Kansl1 Cause K1 Mutations K1 Delineation K1 Spectrum JF American Journal of Medical Genetics Part A LK http://dx.doi.org/https://hdl.handle.net/11499/51017 DO https://hdl.handle.net/11499/51017 SF ELIB - SuUB Bremen
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