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Genetic services in Chile.
Community Genet. 2004;7(2-3):121-5. doi: 10.1159/000080781.
Community Genet. 2004.
PMID: 15539827
Beare-Stevenson syndrome: Two South American patients with FGFR2 analysis.
Vargas RA, Maegawa GH, Taucher SC, Leite JC, Sanz P, Cifuentes J, Parra M, Muñoz H, Maranduba CM, Passos-Bueno MR.
Vargas RA, et al. Among authors: taucher sc.
Am J Med Genet A. 2003 Aug 15;121A(1):41-6. doi: 10.1002/ajmg.a.20101.
Am J Med Genet A. 2003.
PMID: 12900900
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[Genetic markers in essential hypertension].
Passalacqua C, Taucher SC.
Passalacqua C, et al. Among authors: taucher sc.
Rev Med Chil. 2010 Jun;138(6):767-72. doi: 10.4067/s0034-98872010000600016.
Rev Med Chil. 2010.
PMID: 20919489
Review.
Spanish.
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A pigmentary skin defect is a new finding in Marshall-Smith syndrome.
Passalacqua C, Melo C, Martín LM, Rojas F, Sanz P, Taucher SC, Aranibar L.
Passalacqua C, et al. Among authors: taucher sc.
Am J Med Genet A. 2011 Aug;155A(8):2015-7. doi: 10.1002/ajmg.a.34076. Epub 2011 Jul 7.
Am J Med Genet A. 2011.
PMID: 21739579
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Multiple malformations in neonatal hemochromatosis.
Taucher SC, Bentjerodt R, Hübner ME, Nazer J.
Taucher SC, et al.
Am J Med Genet. 1994 Apr 1;50(2):213-4. doi: 10.1002/ajmg.1320500215.
Am J Med Genet. 1994.
PMID: 8010353
No abstract available.
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Familial congenital diaphragmatic hernia: is an imprinting mechanism involved?
Austin-Ward ED, Taucher SC.
Austin-Ward ED, et al. Among authors: taucher sc.
J Med Genet. 1999 Jul;36(7):578-9.
J Med Genet. 1999.
PMID: 10424826
Free PMC article.
No abstract available.
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