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Your search keyword '"Kanya Suphapeetiporn"' showing total 21 results

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21 results on '"Kanya Suphapeetiporn"'

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1. Association of IKZF1 SNPs in cold medicine-related Stevens–Johnson syndrome in Thailand

2. The Thai reference exome (T‐REx) variant database

3. Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand

5. Author response for 'The Thai Reference Exome ( T‐REx ) Variant Database'

6. Association of IKZF1 SNPs in cold medicine-related Stevens–Johnson syndrome in Thailand

7. Author response for 'Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand'

8. Novel mutations in <scp>SPTA</scp> 1 and <scp>SPTB</scp> identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia

9. Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation

10. Novel mutations in Thai patients with glanzmann thrombasthenia

11. Monoallelic FGFR3 and Biallelic ALPL mutations in a Thai girl with hypochondroplasia and hypophosphatasia

12. A novelGJA1mutation in oculodentodigital dysplasia with extensive loss of enamel

13. Gene-Based Meta-Analysis of Genome-Wide Association Study Data Identifies Independent Single-Nucleotide Polymorphisms inANXA6as Being Associated With Systemic Lupus Erythematosus in Asian Populations

14. NovelCTSKmutation resulting in an entire exon 2 skipping in a Thai girl with pycnodysostosis

15. Clinical and Molecular Characterization of Thai Patients with Wiskott-Aldrich Syndrome

16. Holocarboxylase synthetase deficiency: novel clinical and molecular findings

17. Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine disease

18. Carbamazepine and phenytoin induced Stevens-Johnson syndrome is associated with HLA-B*1502 allele in Thai population

19. TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population

20. Expanding the phenotypic spectrum of Caffey disease

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