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1 Ergebnisse
1
MAB21L1 loss of function causes a syndromic neurodevelopmen..:
Rad, Abolfazl
;
Altunoglu, Umut
;
Miller, Rebecca
...
https://freidok.uni-freiburg.de/data/150597. , 2019
Link:
https://freidok.uni-freiburg.de/data/150597
RT Journal T1
MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)
UL https://suche.suub.uni-bremen.de/peid=base-ftunivfreiburg:oai:freidok.uni-freiburg.de:150597&Exemplar=1&LAN=DE A1 Rad, Abolfazl A1 Altunoglu, Umut A1 Miller, Rebecca A1 Maroofian, Reza A1 James, Kiely N A1 Çağlayan, Ahmet Okay A1 Najafi, Maryam A1 Stanley, Valentina A1 Boustany, Rose-Mary A1 Yeşil, Gözde A1 Sahebzamani, Afsaneh A1 Ercan-Sencicek, Gülhan A1 Saeidi, Kolsoum A1 Wu, Kaman A1 Bauer, Peter A1 Bakey, Zeineb A1 Gleeson, Joseph G A1 Hauser, Natalie A1 Gunel, Murat A1 Kayserili, Hulya A1 Schmidts, Miriam YR 2019 JF https://freidok.uni-freiburg.de/data/150597 LK http://dx.doi.org/https://freidok.uni-freiburg.de/data/150597 DO https://freidok.uni-freiburg.de/data/150597 SF ELIB - SuUB Bremen
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