Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

6 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Genetic services in Chile.
Taucher SC. Taucher SC. 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
[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.
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
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.