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| 1 | 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 |
| 2 | 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 |
| 3 | Understanding Niemann Pick Type C Disease, A Fat Problem 显示文摘 | VINCENT I BU B ERICKSON RP | 2003 | Curr Open Neurol (S1350--7540)2003，16，2： | 1 |
| 4 | A familial form of convulsive disor- der with or without mental retardation limited to females : exten- sion of a pedigree limits possible genetic mechanisms 显示文摘 | Fabisiak K Erickson RP | 1990 | Clin Genet1990，38，： | 1 |
| 5 | Uniparental dismy and phenotype of mosaic trisomy 20 : a new case and review of the literature显示文摘 | Powis Z Erickson RP | 2009 | J Appl Genet2009，50，： | 1 |
| 6 | Correction of renal tubular acidosis in carbonic anhydrase 11- deficient mice with gene therapy显示文摘 | Lai LW Chan DM Erickson RP | 1998 | J Clin Invest1998，101，7： | 1 |
| 7 | Autonomic hyperreflexia: pathophysiology and medical management显示文摘 | | 1980 | Arch Phys Med Rehabil1980，61，10： | 1 |
| 8 | Evidence that the serological determinant of H-Y antigen is carbohydrate 显示文摘 | Shapiro M Erickson RP | 1981 | Nature1981，290，5806： | 1 |
| 9 | Isometric and isokinetichip abductor strength in persons with above - knee amputations显示文摘 | Ryser DK Erickson RP Cahalan T | 1988 | Arch Phys Med Rehabil1988，69，10： | 1 |
| 10 | A polymorphism in the 5 # flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E显示文摘 | Baldini M Lohman IC Halonen M Erickson RP Holt PG Martinez FD | 1999 | AmJ Respir Cell Mol Biol1999，20，： | 1 |
| 11 | Creating a conditional mutation of Wnt-1 by antisense transgenesis provides evidence that Wnt-1 is not essential for spermatogenesis显示文摘 | Erickson RP Lai LW Grimes J | 1993 | Dev Genet1993，14，4： | 1 |
| 12 | Current controversies in Niemann-Pick C1 disease: steroids or gangliosides; neurons or neurons and glia显示文摘 | Erickson RP | 2013 | Appl Genet2013，54，2： | 1 |
| 13 | The absence of mitochondrial thioredoxin 2 causes massive apoptosis, exencephaly, and early embryonic lethality in homozygous mice 显示文摘 | Nonn L Williams RR Erickson RP | 2003 | Mol Cell Biol2003，23，3： | 1 |
| 14 | Understanding Niemann-Pick Type C Disease:A Fat Problem显示文摘 | VINCENT I BU BT ERICKSON RP | 2003 | Curr Opin Neurol(S1350-7540)2003，16，： | 1 |
| 15 | 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 |
| 16 | Genes,environment,and orofacial clefting:N-acetyltransferase and folic acid显示文摘 | Erickson RP | | 0，，05： | 1 |
| 17 | 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 |
| 18 | Variable presentation of Rothmund-Thomson syndrome显示文摘 | Pujol LA Erickson RP Heidenreich RA | 2000 | Am J Med Genet2000，95，3： | 1 |
| 19 | Decreased NPC1 gene dosage in mice is associated with weight gain 显示文摘 | Jelinek D Heidenreich RA Erickson RP | 2010 | Obesity(Silver Spring)2010，18，7： | 1 |
| 20 | The absence of mitochondrial thioredoxin 2 causes massive apoptosis,exencephaly,and early embryonic lethality in homozygous mioe显示文摘 | Norm L Williams RR Erickson RP | 2003 | Mol Cell Biol2003，23，3： | 1 |
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