نتائج البحث - Maryam Mokhtarzadeh
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Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center حسب Brian P. Brooks, Wadih M. Zein, A. Thompson, Maryam Mokhtarzadeh, Dan Doherty, Melissa A. Parisi, Ian Glass, May Christine V. Malicdan, Thierry Vilboux, Meghana Vemulapalli, James C. Mullikin, William A. Gahl, Meral Gunay‐Aygun
منشور في 2018Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Medicine
Ophthalmology
Anatomy
Biochemistry
Cell biology
Confocal
Confocal microscopy
Cornea
Cytology
Enzyme
Erg
Fluorescein
Fluorescence
Fluorescence microscope
Fundus (uterus)
Gene
Genetics
Glycosidic bond
Glycosyltransferase
Mutagenesis
Mutation
Optics
Pathology
Physics
Ptosis
Retinal
Staining
Strabismus
Transferase