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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
2023 0

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Search Results

111 results

Results by year

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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.
Trisomy 7p: report of 2 patients and literature review.
Arens YH, Toutain A, Engelen JJ, Offermans JP, Hamers AJ, Schrander JJ, Pulles-Heintzberger CF, Schrander-Stumpel CT. Arens YH, et al. Among authors: schrander stumpel ct. Genet Couns. 2000;11(4):347-54. Genet Couns. 2000. PMID: 11140412 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
Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
Schrander-Stumpel CT, Govaerts LC, Engelen JJ, van der Blij-Philipsen M, Borghgraef M, Loots WJ, Peters JJ, Rijnvos WP, Smeets DF, Fryns JP. Schrander-Stumpel CT, et al. Am J Med Genet. 1994 May 1;50(4):377-80. doi: 10.1002/ajmg.1320500416. Am J Med Genet. 1994. PMID: 7516121 Review.
111 results