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

Results by year

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

Year Number of Results
1985 2
1987 1
1990 3
1991 2
1992 3
1993 4
1994 2
1995 6
1996 4
1997 2
1998 8
1999 4
2000 8
2001 2
2002 2
2003 4
2004 6
2005 7
2006 3
2007 3
2008 8
2009 6
2010 10
2011 7
2012 8
2013 4
2014 3
2015 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

111 results

Results by year

Filters applied: . Clear all
Page 1
Triple X syndrome: a review of the literature.
Otter M, Schrander-Stumpel CT, Curfs LM. Otter M, et al. Among authors: schrander stumpel ct. Eur J Hum Genet. 2010 Mar;18(3):265-71. doi: 10.1038/ejhg.2009.109. Epub 2009 Jul 1. Eur J Hum Genet. 2010. PMID: 19568271 Free PMC article. Review.
Expressive language in children with Kabuki syndrome.
Defloor T, van Borsel J, Schrander-Stumpel CT, Curfs LM. Defloor T, et al. Among authors: schrander stumpel ct. Am J Med Genet A. 2005 Jan 30;132A(3):256-9. doi: 10.1002/ajmg.a.30333. Am J Med Genet A. 2005. PMID: 15578615
Oculoauriculovertebral spectrum and cerebral anomalies.
Schrander-Stumpel CT, de Die-Smulders CE, Hennekam RC, Fryns JP, Bouckaert PX, Brouwer OF, da Costa JJ, Lommen EJ, Maaswinkel-Mooy PD. Schrander-Stumpel CT, et al. J Med Genet. 1992 May;29(5):326-31. doi: 10.1136/jmg.29.5.326. J Med Genet. 1992. PMID: 1583660 Free PMC article. Review.
Cutaneous clues for diagnosing X-chromosomal disorders.
Vreeburg M, Sallevelt SC, Stegmann AP, van Geel M, Detisch YJ, Schrander-Stumpel CT, van Steensel MA, Marcus-Soekarman D. Vreeburg M, et al. Among authors: schrander stumpel ct. Clin Genet. 2014 Apr;85(4):328-35. doi: 10.1111/cge.12162. Epub 2013 Aug 14. Clin Genet. 2014. PMID: 23578112
Acampomelic campomelic syndrome.
Moog U, Jansen NJ, Scherer G, Schrander-Stumpel CT. Moog U, et al. Among authors: schrander stumpel ct. Am J Med Genet. 2001 Dec 1;104(3):239-45. Am J Med Genet. 2001. PMID: 11754051
Lymphedema in Prader-Willi syndrome.
Heitink MV, Sinnema M, van Steensel MA, Schrander-Stumpel CT, Frank J, Curfs LM. Heitink MV, et al. Among authors: schrander stumpel ct. Int J Dermatol. 2008 Nov;47 Suppl 1:42-4. doi: 10.1111/j.1365-4632.2008.03959.x. Int J Dermatol. 2008. PMID: 18986486
111 results