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| 1 | Maternal genome-wide DNA methylation patterns and congenital heart defects 显示文摘 | CHOWDHURY S ERICKSON SW MACLEOD SL | 2011 | PLoSOne2011，6，16： | 1 |
| 2 | Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema- distichiasis syndrome 显示文摘 | Dagenais SL Hartsough RL Erickson RP | 2004 | Gene Expr Patterns2004，4，6： | 1 |
| 3 | Mutations in Fox c2 (MFH-1), a forkhcad family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome 显示文摘 | Fang JM Dagenais SL Erickson RP | 2000 | Am J Hum Genet2000，67，6： | 1 |
| 4 | Maternal genome-wide DNA methylation panerns and congenital heart defects显示文摘 | Chowdhury S Erickson SW MacLeod SL | 2011 | PLoS One2011，6，16： | 1 |
| 5 | Maternal genomewide DNA methylation patterns and congenital heart defects显示文摘 | Chowdhury S Erickson SW Mac Leod SL | 2011 | PLo S One2011，6，16： | 1 |
| 6 | Decreased sensitivity to tumor necrosis factor but normal T-cell development in TNF receptor-2-deficient mice显示文摘 | Erickson SL De Sauvage FJ Kikly K | 1994 | Nature1994，372，6506： | 1 |
| 7 | Decreas~ed-/ssensitiv- ity to tumour-necrosis factor but normal T-cell development in TNF receptor-2 deficient mice 显示文摘 | Erickson SL de Sauvage FJ Kikly K | 1994 | Nature1994，372，6506： | 1 |
| 8 | Risk factors for trisomy 21 : maternal cigarette smoking and oral contraceptive use in a population - based case control study显示文摘 | Yang Q Sherman SL Hassold TJ Allran K Taft LF Pettay D Khoury MJ Erickson JD Freeman SB | 1999 | Genet Med1999，1，： | 1 |
| 9 | Maternal genorne- wide DNA methylation patterns and congenital heart defects 显示文摘 | Chowdhury S Erickson SW MacLeod SL | 2011 | 24 (1) :e 165062011，24，16： | 1 |
| 10 | Maternal genome-wideDNA methylation patterns and congenital heart defects显示文摘 | Chowdhury S Erickson SW Macleod SL | | 0，，01： | 1 |
| 11 | Dopamine innervation of the monkey mediodorsal thalamus : Location of projection neurons and ultrastructural characteristics of axon terminals显示文摘 | Melchitzky DS Erickson SL Lewis DA | 2006 | Neuroscience2006，143，4： | 1 |
| 12 | Ma- ternal genome-wide DNA methylation patterns and congenital heart defects显示文摘 | Chowdhury S Erickson SW Macleod SL | 2011 | PLoS One2011，6，1： | 1 |
| 13 | Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome 显示文摘 | Fang J Dagenais SL Erickson RP | 2000 | AmJ Hum Genet2000，67，6： | 1 |
| 14 | Mutations in FOXC2(MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome显示文摘 | Dagenais SL Erickson RP | 2000 | Am J Hum Genet2000，67，6： | 1 |
| 15 | Analysis of the effectiveness of in-office and transtelephonic follow-up in terms of pace- maker system complications显示文摘 | Sweesy MW Erickson SL Crago JA | 1994 | Pacing Clin Electrophysiol1994，17，112： | 1 |
| 16 | Mutations in FOXC2(MFH-1),a forkhead family transcription factor,are responsible for the hereditary lymphedema-distichiasis syndrome显示文摘 | Fang J Dagenais SL Erickson RP | 2000 | Am J Hum Genet2000，67，6： | 1 |
| 17 | Mutations in FOXC2 (MFH-1),a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome显示文摘 | Fang J Dagenais SL Erickson RP | 2000 | An J Hum Genet2000，67，6： | 1 |
| 18 | Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutation显示文摘 | Erickson RP Dagenais SL Caulder MS | 2001 | J Med Genet2001，38，11： | 1 |
| 19 | Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedcma-d/stichia- sis syndrome显示文摘 | Fang J Dagenais SL Erickson RP | 2000 | Am J Hum Genet2000，67，6： | 1 |
| 20 | Matemal ge- nome-wide DNA methylation patterns and congenital heart defects 显示文摘 | Chowdhury S Erickson SW MacLeod SL | 2011 | PloSOne2011，6，16： | 1 |
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