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Publications by Dilyara N. Gubaeva
Hypopituitarism Due to Mutation in the PROP1 Gene in Association With the 47,XYY Karyotype and Autosomal Dominant Atrioventricular Septal Defect: Two Case Reports
Problemy Endokrinologii
Endocrinology
Metabolism
Diabetes
Related publications
Autosomal Dominant Macular Degeneration Associated With 208del G Mutation in the FSCN2 Gene
Archives of Ophthalmology
A Case of Autosomal Dominant Osteopetrosis Type II With a CLCN7 Gene Mutation
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Phenotypic Variability in Autosomal Dominant Familial Alzheimer Disease Due to the S170F Mutation of Presenilin-1
Neurodegenerative Diseases
Neurology
P55 a Case of Vein of Galen Malformation With Atrioventricular Septal Defect
Right-Sided Infective Endocarditis in Patients With Uncorrected Ventricular Septal Defect and Patent Ductus Arteriosus: Two Case Reports
Clinical Case Reports
Medicine
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
A Patient With a Novel Gene Mutation Leading to Autosomal Dominant Polycystic Kidney Disease
Clinical Journal of the American Society of Nephrology
Epidemiology
Nephrology
Critical Care
Transplantation
Intensive Care Medicine
A Man With 47,XYY Karyotype, Prolactinoma and a History of First Trimester Recurrent Miscarriages in His Wife
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Phenotype of Autosomal Dominant Cone–rod Dystrophy Due to the R838C Mutation of the GUCY2D Gene Encoding Retinal Guanylate Cyclase-1
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
