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| 1 | The genetics of common disorders-congenital diaphrag- matic hernia显示文摘 | Slavotinek AM | 2014 | Eur J Ned Genet2014，57，8： | 1 |
| 2 | Novel microdeletion syndromes detected by chromosome microarrays 显示文摘 | Slavotinek AM | 2008 | Human Genetics2008，124，1： | 1 |
| 3 | Report of a child with aortic aneurysm,orofacial clefting,hemangioma,upper sternal defect,and marfanoid features:possible PHACE syndrome显示文摘 | Slavotinek AM Dubovsky E Dietz HC | 2002 | Am J Med Genet2002，110，3： | 1 |
| 4 | Report of a child with aortic aneurysm, orofaeial clefting, hemangioma, upper sternal de fect, and marfanoid features: possible PHACE syndrome显示文摘 | Slavotinek AM Dubovsky E Dietz HC | 2002 | Am J Med Genet2002，110，3： | 1 |
| 5 | Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal de fect,and marfanoid features: possible PHACE syndrome显示文摘 | Slavotinek AM Dubovsky E Dietz HC | 2002 | Am J Med Genet2002，110，3： | 1 |
| 6 | VAX1 mutation associated with mierophthalmia, corpus callosum agenesis, and orofaeial clefting:the first description of a V AX1 phenotype in humans显示文摘 | Slavotinek AM Chao R Vacik T | 2012 | Hum Mutat2012，33，2： | 1 |
| 7 | Eye development genes and known syndromes显示文摘 | Slavotinek AM | | 0，，： | 1 |
| 8 | Novel microdeletion syndromes detected by chromosome microarrays显示文摘 | Slavotinek AM | 2008 | Hum Genet2008，124，： | 1 |
| 9 | The genetics of congenital diaphragmatic hernia显示文摘 | Slavotinek AM | 2005 | Semin Perinatol2005，29，： | 1 |
| 10 | Mutations in MKKS cause Bardet-Biedl syndrome显示文摘 | Slavotinek AM Stone EM Mykytyn K | 2000 | Nat Genet2000，26，： | 1 |
| 11 | Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63 显示文摘 | Slavotinek AM Tanaka J Winder A | 2005 | Am J Med Genet2005，138，： | 1 |
| 12 | Eye development genes and known syndromes 显示文摘 | Slavotinek AM | 2011 | Mol Genet Metab2011，104，7： | 1 |
| 13 | VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans 显示文摘 | Slavotinek AM Chao R Vacik T | 2012 | Hum mutat2012，33，2： | 1 |
| 14 | Sudden death caused by pulmonary thromboembolism in Proteus syndrome显示文摘 | Slavotinek AM Vacha SJ Peters KF | 2001 | Clin Genet2001，58，： | 1 |
| 15 | Mutations in MKKS cause Bardet-Biedl syndrome 显示文摘 | Slavotinek AM Stone EM Mykytyn K | 2000 | Nat Genet2000，26，1： | 1 |
| 16 | Novel microdeletion syndromes detected by chromosome microarrays显示文摘 | Slavotinek AM | 2008 | Hum Genet2008，124，1： | 1 |
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