Schrander-Stumpel C - Search Results

1

Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling.

Schrander-Stumpel C, Fryns JP. Schrander-Stumpel C, et al. Eur J Pediatr. 1998 May;157(5):355-62. doi: 10.1007/s004310050830. Eur J Pediatr. 1998. PMID: 9625330 Review.

2

[From gene to disease; X-linked hydrocephalus and LiCAM].

Schrander-Stumpel CT, Vos YJ. Schrander-Stumpel CT, et al. Ned Tijdschr Geneeskd. 2004 Jul 17;148(29):1441-3. Ned Tijdschr Geneeskd. 2004. PMID: 15326648 Review. Dutch.

3

Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child.

Staals JE, Schrander-Stumpel CT, Hamers G, Fryns JP. Staals JE, et al. Genet Couns. 2003;14(2):233-7. Genet Couns. 2003. PMID: 12872819 Review.

4

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

5

Adducted thumbs: a clinical clue to genetic diagnosis.

Verhagen JM, Schrander-Stumpel CT, Blezer MM, Weber JW, Schrander JJ, Rubio-Gozalbo ME, Bakker JA, Stegmann AP, Vos YJ, Frints SG. Verhagen JM, et al. Among authors: schrander stumpel ct. Eur J Med Genet. 2013 Mar;56(3):153-8. doi: 10.1016/j.ejmg.2012.11.004. Epub 2012 Dec 7. Eur J Med Genet. 2013. PMID: 23220544

6

Congenital hydrocephalus in clinical practice: a genetic diagnostic approach.

Verhagen JM, Schrander-Stumpel CT, Krapels IP, de Die-Smulders CE, van Lint FH, Willekes C, Weber JW, Gavilanes AW, Macville MV, Stegmann AP, Engelen JJ, Bakker J, Vos YJ, Frints SG. Verhagen JM, et al. Eur J Med Genet. 2011 Nov-Dec;54(6):e542-7. doi: 10.1016/j.ejmg.2011.06.005. Epub 2011 Jul 30. Eur J Med Genet. 2011. PMID: 21839187

7

Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).

Moog U, Smeets EE, van Roozendaal KE, Schoenmakers S, Herbergs J, Schoonbrood-Lenssen AM, Schrander-Stumpel CT. Moog U, et al. Eur J Paediatr Neurol. 2003;7(1):5-12. doi: 10.1016/s1090-3798(02)00134-4. Eur J Paediatr Neurol. 2003. PMID: 12615169 Review.

8

Different distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly.

Sinnema M, van Roozendaal KE, Maaskant MA, Smeets HJ, Engelen JJ, Jonker-Houben N, Schrander-Stumpel CT, Curfs LM. Sinnema M, et al. Eur J Hum Genet. 2010 Sep;18(9):993-8. doi: 10.1038/ejhg.2010.67. Epub 2010 May 12. Eur J Hum Genet. 2010. PMID: 20461108 Free PMC article.

9

Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype.

Marcus-Soekarman D, Hamers G, Mulder AL, Offermans J, Offermans J, Engelen J, van Lent-Albrechts JC, Robben SG, de Muinck Keizer-Schrama S, Wolffenbuttel KP, Looijenga LH, Oosterhuis JW, Schrander-Stumpel C, Nijhuis J. Marcus-Soekarman D, et al. Prenat Diagn. 2005 Apr;25(4):279-82. doi: 10.1002/pd.996. Prenat Diagn. 2005. PMID: 15849784

10

Hyperechogenic fetal bowel: counseling difficulties.

Marcus-Soekarman D, Offermans J, Van den Ouweland AM, Mulder AL, Muntjewerff N, Vossen M, Kleijer W, Schrander-Stumpel C, Dooijes D. Marcus-Soekarman D, et al. Eur J Med Genet. 2005 Oct-Dec;48(4):421-5. doi: 10.1016/j.ejmg.2005.05.001. Eur J Med Genet. 2005. PMID: 16378926

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