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Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 8, p. 613, doi. 10.1038/sj.ejhg.5200508
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- Article
Mutant WD-repeat protein in triple-A syndrome.
- Published in:
- Nature Genetics, 2000, v. 26, n. 3, p. 332, doi. 10.1038/81642
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- Article
A Homozygous Mutation of Prelamin-A Preventing Its Farnesylation and Maturation Leads to a Severe Lipodystrophic Phenotype: New Insights into the Pathogenicity of Nonfarnesylated Prelamin-A.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 5, p. E856, doi. 10.1210/jc.2010-2234
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- Article
Pituitary apoplexy after somatostatin analogue administration: coincidental or causative?
- Published in:
- Clinical Endocrinology, 2014, v. 81, n. 3, p. 471, doi. 10.1111/cen.12339
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- Article