Found: 6
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Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1–Xp21.3 mental retardation.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 2, p. 87, doi. 10.1038/sj.ejhg.5200415
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- Publication type:
- Article
Transient Neonatal Diabetes Mellitus in a Child with Paternal Uniparental Disomy of Chromosome 6.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 7, p. 893, doi. 10.1515/jpem.2001.14.7.893
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- Article
Transient Neonatal Diabetes.
- Published in:
- Diabetes, 2000, v. 49, n. 8, p. 1359, doi. 10.2337/diabetes.49.8.1359
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- Publication type:
- Article
An imprinted locus associated with transient neonatal diabetes mellitus.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 4, p. 589, doi. 10.1093/hmg/9.4.589
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- Publication type:
- Article
Searching for the 1 in 2,400,000: A review of dystrophin gene point mutations.
- Published in:
- Human Mutation, 1994, v. 4, n. 1, p. 1, doi. 10.1002/humu.1380040102
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- Publication type:
- Article
Further Evidence for an Imprinted Gene for Neonatal Diabetes Localised to Chromosome 6q22–q23.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1117, doi. 10.1093/hmg/5.8.1117
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- Publication type:
- Article