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Publications by S Holloway
Probably Norrie's Disease Due to Mutation. Two Sporadic Sibships of Two Males Each, a Necropsy of One Case, And, Given Norrie's Disease, a Calculation of the Gene Mutation Frequency.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Related publications
Bilateral Norrie's Disease in Identical Twins.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Norrie's Disease in an Asian Family.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Case of the Mosaicism in the Silkworm Egg, Probably Due to a Recessive Mutation
The Japanese journal of genetics
A Probable Case of Mutation in Huntington's Disease.
Journal of Medical Genetics
Genetics
Case Report: Maple Syrup Urine Disease With a Novel DBT Gene Mutation
BMC Pediatrics
Child Health
Pediatrics
Perinatology
Disruption of Copper Homeostasis Due to a Mutation of Atp7a Delays the Onset of Prion Disease
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
PRRT2 Mutation in a Sporadic Case of Paroxysmal Kinesigenic Dyskinesia
Juntendo Medical Journal
Juvenile Onset Autoinflammatory Disease Due to a Novel Mutation in TNFAIP3 (A20)
Arthritis Research & Therapy
Cystic Fibrosis Gene Mutation in Two Sisters With Mild Disease and Normal Sweat Electrolyte Levels
New England Journal of Medicine
Medicine
