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Publications by Jannet González

Deep Genotyping of the IDS Gene in Colombian Patients With Hunter Syndrome

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2014English

Related publications

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report

Frontiers in Genetics
GeneticsMolecular Medicine
2020English

Genotyping FOXG1 Mutations in Patients With Clinical Evidence of the FOXG1 Syndrome

Molecular Syndromology
Genetics
2012English

Mutations in the FGFR2 Gene in Mexican Patients With Apert Syndrome

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2015English

The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1973English

Image Gallery: Cutaneous Findings in Hunter Syndrome

British Journal of Dermatology
DermatologyMedicine
2018English

Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome

Journal of Human Genetics
Genetics
2000English

Antiphosphatidylethanolamine Antibodies and Deep Vein Thrombosis in Lupus Patients With Antiphospholipid Syndrome

Revista Romana de Medicina de Laborator
2018English

Genotyping Patients With Recent Blood Transfusions

Epidemiology
Epidemiology
2003English

PTPN22 C1858T Polymorphism in Colombian Patients With Autoimmune Diseases

Genes and Immunity
ImmunologyGenetics
2005English

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