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Publications by Katie Stoll
Homozygous 15q13.3 Microdeletion in a Child With Hypotonia and Impaired Vision: A New Report and Review of the Literature
Clinical Case Reports
Medicine
Related publications
Delineating the 15q13.3 Microdeletion Phenotype: A Case Series and Comprehensive Review of the Literature
Genetics in Medicine
Medicine
Genetics
Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review
Case Reports in Pediatrics
A Novel Homozygous Frame-Shift Mutation in the SLC29A3 Gene: A New Case Report and Review of Literature
BMC Medical Genetics
Genetics
Urolithiasis in a Child With Acute Lymphoblastic Leukemia - A Case Report and Review of Literature
Pediatric Review: International Journal of Pediatric Research
Jaguar Attack on a Child: Case Report and Literature Review
Western Journal of Emergency Medicine
Medicine
Emergency Medicine
Otogenic Temporomandibular Septic Arthritis in a Child: A Case Report and a Review of the Literature
Italian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Childhood Stroke and Vision: A Review of the Literature
Pediatric Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Post-Traumatic Leptomeningeal Cyst in Child: A Case Report and Review of Literature
International Journal of Case Reports in Medicine
Microdeletion of 6q16.1 Encompassing EPHA7 in a Child With Mild Neurological Abnormalities and Dysmorphic Features: Case Report
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology