Found: 4
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The phenotype of a 45, X male with a Y/18 translocation.
- Published in:
- Clinical Genetics, 1996, v. 49, n. 1, p. 37, doi. 10.1111/j.1399-0004.1996.tb04322.x
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- Article
Parental Origin of G<sub>s</sub>α Mutations in the McCune-Albright Syndrome and in Isolated Endocrine Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 6, p. 3007, doi. 10.1210/jc.2004-0194
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- Publication type:
- Article
Different Inactivating Mutations of the Mineralocorticoid Receptor in Fourteen Families Affected by Type I Pseudohypoaldosteronism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 6, p. 2508, doi. 10.1210/jc.2002-021932
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- Publication type:
- Article
Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 1, p. 76, doi. 10.1038/sj.ejhg.5201719
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- Article