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FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
Hum Mol Genet. 2003 May 15;12(10):1179-85. doi: 10.1093/hmg/ddg123.
Hum Mol Genet. 2003.
PMID: 12719382
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.
Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW.
Erickson RP, et al. Among authors: caulder ms.
J Med Genet. 2001 Nov;38(11):761-6. doi: 10.1136/jmg.38.11.761.
J Med Genet. 2001.
PMID: 11694548
Free PMC article.
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Mutation of the FOXC2 gene in familial distichiasis.
Brooks BP, Dagenais SL, Nelson CC, Glynn MW, Caulder MS, Downs CA, Glover TW.
Brooks BP, et al. Among authors: caulder ms.
J AAPOS. 2003 Oct;7(5):354-7. doi: 10.1016/s1091-8531(03)00144-7.
J AAPOS. 2003.
PMID: 14566319
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Family history, diabetes, and other demographic and risk factors among participants of the National Health and Nutrition Examination Survey 1999-2002.
Annis AM, Caulder MS, Cook ML, Duquette D.
Annis AM, et al. Among authors: caulder ms.
Prev Chronic Dis. 2005 Apr;2(2):A19. Epub 2005 Mar 15.
Prev Chronic Dis. 2005.
PMID: 15888230
Free PMC article.
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The Impact of COVID-19 on the All of Us Research Program.
Hedden SL, McClain J, Mandich A, Baskir R, Caulder MS, Denny JC, Hamlet MRJ, Prabhu Das I, McNeil Ford N, Lopez-Class M, Elmi A, Wallace R, Linkie A, Garriock HA.
Hedden SL, et al. Among authors: caulder ms.
Am J Epidemiol. 2023 Jan 6;192(1):11-24. doi: 10.1093/aje/kwac169.
Am J Epidemiol. 2023.
PMID: 36205043
Free PMC article.
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