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Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia.
- Published in:
- Neurogenetics, 2007, v. 8, n. 1, p. 51, doi. 10.1007/s10048-006-0069-6
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- Publication type:
- Article
Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia.
- Published in:
- 2007
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- Publication type:
- Correction notice
Waardenburg Syndrome Type I with Heterochromia Iridis and Circumscribed Hypopigmentation of the Skin.
- Published in:
- Pediatric Dermatology, 2009, v. 26, n. 6, p. 759, doi. 10.1111/j.1525-1470.2009.01033.x
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- Publication type:
- Article
Mutations in the PDS Gene in German Families with Pendred’s Syndrome: V138F Is a Founder Mutation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 6, p. 2916, doi. 10.1210/jc.2002-021334
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- Publication type:
- Article