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Publications by Andreas Gal
Clinical Utility Gene Card For: Fabry Disease
European Journal of Human Genetics
Genetics
Clinical Utility Gene Card For: Adrenoleukodystrophy
European Journal of Human Genetics
Genetics
A Novel Stop Mutation (P.(Gln22*)) of DAX1 (NR0B1) Results in Late-Onset X-Linked Adrenal Hypoplasia Congenita
Endocrinology, Diabetes and Metabolism Case Reports
Internal Medicine
Endocrinology
Metabolism
Diabetes
Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, With Homoallelism for Mutations in RPE65 or MERTK, Respectively
American Journal of Human Genetics
Genetics