Found: 7
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Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndrome.
- Published in:
- European Journal of Immunology, 2011, v. 41, n. 4, p. 1120, doi. 10.1002/eji.201040909
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- Publication type:
- Article
FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 3, p. 157, doi. 10.1038/sj.ejhg.5200425
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- Publication type:
- Article
Deletion of NSD1 exon 14 in Sotos syndrome: first description.
- Published in:
- Journal of Genetics, 2011, v. 90, n. 1, p. 119, doi. 10.1007/s12041-011-0017-6
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- Publication type:
- Article
The H1 Haplotype of the Tau Gene (MAPT) is Associated with Mild Cognitive Impairment.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 19, n. 3, p. 909, doi. 10.3233/JAD-2010-1285
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- Publication type:
- Article
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 18, doi. 10.1038/83707
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- Publication type:
- Article
Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
- Published in:
- 2006
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- Publication type:
- journal article
Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21q.
- Published in:
- British Journal of Haematology, 1998, v. 103, n. 1, p. 213, doi. 10.1046/j.1365-2141.1998.00924.x
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- Publication type:
- Article