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Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 7, p. 799, doi. 10.1515/jpem-2018-0023
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- Publication type:
- Article
Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.
- Published in:
- Endocrine (1355008X), 2021, v. 71, n. 1, p. 189, doi. 10.1007/s12020-020-02494-z
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- Publication type:
- Article
Genotype‐phenotype correlation of K<sub>ATP</sub> channel gene defects causing permanent neonatal diabetes in Indian patients.
- Published in:
- Pediatric Diabetes, 2021, v. 22, n. 1, p. 82, doi. 10.1111/pedi.13109
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- Publication type:
- Article
Small for gestation and growth hormone therapy.
- Published in:
- 2006
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- Publication type:
- journal article