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1.
Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects.
Eur J Med Genet
; 49(2): 151-8, 2006.
Artículo
en Inglés
| MEDLINE | ID: mdl-16530712
2.
Characterisation and expression analysis of the WDR9 gene, located in the Down critical region-2 of the human chromosome 21.
Biochim Biophys Acta
; 1577(3): 377-83, 2002 Sep 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-12359327
3.
The identification of a novel human homologue of the SH3 binding glutamic acid-rich (SH3BGR) gene establishes a new family of highly conserved small proteins related to Thioredoxin Superfamily.
Gene
; 291(1-2): 233-9, 2002 May 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-12095696
4.
TBX3, the gene mutated in ulnar-mammary syndrome, promotes growth of mammary epithelial cells via repression of p19ARF, independently of p53.
Cell Tissue Res
; 328(2): 301-16, 2007 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-17265068
5.
The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouse.
Mol Cell Neurosci
; 22(4): 530-43, 2003 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-12727448
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