A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency | Zendy

Malik Ejder Yıldırım | Zendy

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A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency

Author(s) -

Malik Ejder Yıldırım

Publication year - 2018

Publication title -

the annals of clinical and analytical medicine

Language(s) - English

Resource type - Journals

ISSN - 2667-663X

DOI - 10.4328/jcam.5718

Subject(s) - medicine , pediatrics , mutation , ectopia lentis , surgery , genetics , gene , biology , marfan syndrome

1 Malik Ejder Yıldırım1, Ayşe Vural2, Hande Küçük Kurtulgan1, Hasan Kılıçgün3, Burak Başer1 1Department of Medical Genetics, Cumhuriyet University, Faculty of Medicine, Sivas, 2Department of Ophthalmology, Cumhuriyet University, Faculty of Medicine, Sivas, 3 Department of Nutrition and Dietetics, Erzincan University, Faculty of Health Sciences, Erzincan, Turkey A case of weill-marchesani syndrome A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency

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