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Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome.
- Published in:
- Frontiers in Endocrinology, 2019, v. 10, p. 1, doi. 10.3389/fendo.2019.00864
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- Article
Establishing a Standardized DNA Extraction Method Using NaCl from Oral Mucosa Cells for Its Application in Imprinting Diseases Such as Prader–Willi and Angelman Syndromes: A Preliminary Investigation.
- Published in:
- Genes, 2024, v. 15, n. 5, p. 641, doi. 10.3390/genes15050641
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- Article
Investigating the correlation between genotype and phenotype in Prader-Willi syndrome: a study of 45 cases from Brazil.
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- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03157-2
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- Article
A rapid and accurate methylation‐sensitive high‐resolution melting analysis assay for the diagnosis of Prader Willi and Angelman patients.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.637
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- Article