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

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1887 1
1913 1
1918 1
1979 1
1982 1
1986 1
1987 2
1988 3
1989 2
1991 2
1993 2
1995 3
1996 1
1998 2
2001 2
2003 1
2004 2
2005 5
2006 1
2007 5
2008 5
2009 11
2010 8
2011 11
2012 8
2013 12
2014 11
2015 8
2016 14
2017 5
2018 7
2019 7
2020 8
2021 6
2022 11
2023 6
2024 0

Text availability

Article attribute

Article type

Publication date

Similar articles for PMID: 24357603

152 results

Results by year

Filters applied: . Clear all
Page 1
Focal dermal hypoplasia without focal dermal hypoplasia.
Contreras-Capetillo SN, Lombardi MP, Pinto-Escalante D, Hennekam RC. Contreras-Capetillo SN, et al. Am J Med Genet A. 2014 Mar;164A(3):778-81. doi: 10.1002/ajmg.a.36341. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357603
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
Harmsen MB, Azzarello-Burri S, García González MM, Gillessen-Kaesbach G, Meinecke P, Müller D, Rauch A, Rossier E, Seemanova E, Spaich C, Steiner B, Wieczorek D, Zenker M, Kutsche K. Harmsen MB, et al. Eur J Hum Genet. 2009 Oct;17(10):1207-15. doi: 10.1038/ejhg.2009.40. Epub 2009 Mar 11. Eur J Hum Genet. 2009. PMID: 19277062 Free PMC article.
Focal dermal hypoplasia (Goltz-Gorlin syndrome): a new case with a novel variant in the PORCN gene (c.1250T>C:p.F417S) and unusual spinal anomaly.
Garavelli L, Simonte G, Rosato S, Wischmeijer A, Albertini E, Guareschi E, Longo C, Albertini G, Gelmini C, Greco C, Errico S, Savino G, Pavanello M, Happle R, Unger S, Superti-Furga A, Grzeschik KH. Garavelli L, et al. Am J Med Genet A. 2013 Jul;161A(7):1750-4. doi: 10.1002/ajmg.a.35964. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696273
Goltz syndrome and PORCN: A view from Europe.
Happle R. Happle R. Am J Med Genet C Semin Med Genet. 2016 Mar;172C(1):21-3. doi: 10.1002/ajmg.c.31469. Epub 2016 Jan 22. Am J Med Genet C Semin Med Genet. 2016. PMID: 26799923 Review.
152 results