Found: 4
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MEN2A-RET-induced cellular transformation by activation of STAT3.
- Published in:
- Oncogene, 2001, v. 20, n. 38, p. 5350, doi. 10.1038/sj.onc.1204715
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- Publication type:
- Article
Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 8, p. 604, doi. 10.1038/sj.ejhg.5201199
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- Publication type:
- Article
SMA carrier testing – validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 2, p. 79, doi. 10.1038/sj.ejhg.5200404
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- Publication type:
- Article
A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 4, p. 478, doi. 10.1038/sj.ejhg.5200334
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- Publication type:
- Article