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| 1 | Autosomal dominant spondyIocostal dysostosis is caused by mutation in TBX6显示文摘 | Sparrow DB McInerney-Leo A Gucev ZS | 2013 | Hum Mol Genet2013，22，8： | 1 |
| 2 | A case of Silver-Russell syn- drome( SRS ) : multiple pituitary hormone deficiency, lack of H19 hypomethylation and favourable growth hormone ( GH ) treatment re- sponse显示文摘 | Gucev ZS Tasic V Jancevska A | 2009 | J Genet2009，88，2： | 1 |
| 3 | Autosomaldominant spondylocostal dysostosis in three generations of amacedonian family:negative mutation analysis of DLL3,MESP2,HES7,and LFNG显示文摘 | Gucev ZS Tasic V Pop-Jordanova N | 2010 | Am J Med Genet(Part A)2010，152，6： | 1 |
| 4 | CLOVE Syndrome (Congenital Lipomatous Overgrowth, Vascular Malforma- tions, and Epidermal Nevi)z CNS Malformations and Sei- zures may be a Component of this Disorder显示文摘 | Gucev ZS Tasic V Jancevska A | 2008 | Am J Med Genet A2008，146，20： | 1 |
| 5 | Insulin-like growth factor binding protein 3 mediates retinoic acid-and transforming growth factor beta2-indueed growth inhibition in human breast cancer cell 显示文摘 | Gucev ZS Oh Y Kelley KM | 1996 | Cancer Res1996，56，： | 1 |
| 6 | Autosomal dominant spondylocostal dysostosis in three generations of a macedonian family:negative mutation analysis of DLL3,MESP2,HES7,and LFNG显示文摘 | Gucev ZS Tasic V Pop-Jordanova N | 2010 | Am J Med Genet2010，152，6： | 1 |
| 7 | Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1, 2-dioxygenase (HGD) 显示文摘 | Gucev ZS Slaveska N Laban N | 2011 | Prilozi2011，32，1： | 1 |
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