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Familial mutation in caffey disease with reduced penetrance..:
Özdemir, Özmert Muhammet Ali
;
Tancer-Elçi, Hazal
;
Polat, Aziz
...
Turkish Journal of Pediatrics. , 2017
Link:
https://hdl.handle.net/11499/9148
RT Journal T1
Familial mutation in caffey disease with reduced penetrance: A case report
UL https://suche.suub.uni-bremen.de/peid=base-ftpamukkaleuniv:oai:gcris.pau.edu.tr:11499_9148&Exemplar=1&LAN=DE A1 Özdemir, Özmert Muhammet Ali A1 Tancer-Elçi, Hazal A1 Polat, Aziz A1 Güçtürk, İinci A1 Tepeli, Emre A1 Zeybek, Selcan A1 Ayaz, Akif PB Turkish Journal of Pediatrics YR 2017 K1 Caffey disease K1 COL1A1 K1 Infant K1 Mutation K1 alkaline phosphatase K1 collagen type 1 K1 ibuprofen K1 indometacin K1 vitamin D K1 Article K1 blood smear K1 bone lesion K1 bone radiography K1 case report K1 clavicle K1 clinical article K1 cortical thickness (bone) K1 crying K1 erythrocyte sedimentation rate K1 familial disease K1 follow up K1 gene K1 genetic analysis K1 head circumference K1 human K1 irritability K1 long bone K1 lower limb K1 male K1 mandible K1 missense mutation K1 ossification K1 penetrance K1 restlessness K1 sequence analysis K1 swelling K1 thrombocytosis K1 tibia K1 type I collagen alpha 1 chain gene K1 upper limb JF Turkish Journal of Pediatrics LK http://dx.doi.org/https://hdl.handle.net/11499/9148 DO https://hdl.handle.net/11499/9148 SF ELIB - SuUB Bremen
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