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Publications by Vorasuk Shotelersuk

Absent Expression of the Osteoblast-Specific Maternally Imprinted Genes,DLX5andDLX6,causes Split Hand/Split Foot Malformation Type I

Journal of Medical Genetics
Genetics
2014English

Novel Mutations in SPTA1 and SPTB Identified by Whole Exome Sequencing in Eight Thai Families With Hereditary Pyropoikilocytosis Presenting With Severe Fetal and Neonatal Anaemia

British Journal of Haematology
Hematology
2018English

Expanding the Oro-Dental and Mutational Spectra of Kabuki Syndrome and Expression of KMT2D and KDM6A in Human Tooth Germs

International Journal of Biological Sciences
Applied MicrobiologyEvolutionEcologyDevelopmental BiologyCell BiologyMolecular BiologySystematicsBehaviorBiotechnology
2018English

Splicing Analysis of CYP11B1 Mutation in a Family Affected With 11β-Hydroxylase Deficiency: Case Report

BMC Endocrine Disorders
MedicineEndocrinologyMetabolismDiabetes
2016English

A Novel De Novo COL1A1 Mutation in a Thai Boy With Osteogenesis Imperfecta Born to Consanguineous Parents

Genetics and Molecular Biology
GeneticsMolecular Biology
2017English

Evidence for Locus Heterogeneity in Puerto Ricans With Hermansky-Pudlak Syndrome

American Journal of Human Genetics
Genetics
1997English

Breakpoint Identification, Detection and Frequency of the 65-Kb Deletion in the Cystinosis Gene, CTNS

Pediatric Research
Child HealthPediatricsPerinatology
1999English

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