Schrijver I - Search Results

1

Prothrombin gene variants in non-Caucasians with fetal loss and intrauterine growth retardation.

Schrijver I, Lenzi TJ, Jones CD, Lay MJ, Druzin ML, Zehnder JL. Schrijver I, et al. J Mol Diagn. 2003 Nov;5(4):250-3. doi: 10.1016/S1525-1578(10)60482-5. J Mol Diagn. 2003. PMID: 14573785 Free PMC article.

2

Homozygous factor V splice site mutation associated with severe factor V deficiency.

Schrijver I, Koerper MA, Jones CD, Zehnder JL. Schrijver I, et al. Blood. 2002 Apr 15;99(8):3063-5. doi: 10.1182/blood.v99.8.3063. Blood. 2002. PMID: 11929802 Free article.

3

Diagnostic single nucleotide polymorphism analysis of factor V Leiden and prothrombin 20210G > A. A comparison of the Nanogen Eelectronic Microarray with restriction enzyme digestion and the Roche LightCycler.

Schrijver I, Lay MJ, Zehnder JL. Schrijver I, et al. Am J Clin Pathol. 2003 Apr;119(4):490-6. doi: 10.1309/3VTR-7TL2-X7TX-L0QY. Am J Clin Pathol. 2003. PMID: 12710121

4

Rapid combined genotyping assay for four achondroplasia and hypochondroplasia mutations by real-time PCR with multiple detection probes.

Schrijver I, Lay MJ, Zehnder JL. Schrijver I, et al. Genet Test. 2004 Summer;8(2):185-9. doi: 10.1089/gte.2004.8.185. Genet Test. 2004. PMID: 15345118

5

Detection of the JAK2 V617F mutation by LightCycler PCR and probe dissociation analysis.

Lay M, Mariappan R, Gotlib J, Dietz L, Sebastian S, Schrijver I, Zehnder JL. Lay M, et al. Among authors: schrijver i. J Mol Diagn. 2006 Jul;8(3):330-4. doi: 10.2353/jmoldx.2006.050130. J Mol Diagn. 2006. PMID: 16825505 Free PMC article.

6

Testing for maternal cell contamination in prenatal samples: a comprehensive survey of current diagnostic practices in 35 molecular diagnostic laboratories.

Schrijver I, Cherny SC, Zehnder JL. Schrijver I, et al. J Mol Diagn. 2007 Jul;9(3):394-400. doi: 10.2353/jmoldx.2007.070017. J Mol Diagn. 2007. PMID: 17591939 Free PMC article.

7

Identification of an intronic single nucleotide polymorphism leading to allele dropout during validation of a CDH1 sequencing assay: implications for designing polymerase chain reaction-based assays.

Mullins FM, Dietz L, Lay M, Zehnder JL, Ford J, Chun N, Schrijver I. Mullins FM, et al. Among authors: schrijver i. Genet Med. 2007 Nov;9(11):752-60. doi: 10.1097/gim.0b013e318159a369. Genet Med. 2007. PMID: 18007144 Free article.

8

Design and evaluation of a real-time PCR assay for quantification of JAK2 V617F and wild-type JAK2 transcript levels in the clinical laboratory.

Merker JD, Jones CD, Oh ST, Schrijver I, Gotlib J, Zehnder JL. Merker JD, et al. Among authors: schrijver i. J Mol Diagn. 2010 Jan;12(1):58-64. doi: 10.2353/jmoldx.2010.090068. Epub 2009 Dec 3. J Mol Diagn. 2010. PMID: 19959796 Free PMC article.

9

Combined use of PCR-based TCRG and TCRB clonality tests on paraffin-embedded skin tissue in the differential diagnosis of mycosis fungoides and inflammatory dermatoses.

Zhang B, Beck AH, Taube JM, Kohler S, Seo K, Zwerner J, Viakhereva N, Sundram U, Kim YH, Schrijver I, Arber DA, Zehnder JL. Zhang B, et al. Among authors: schrijver i. J Mol Diagn. 2010 May;12(3):320-7. doi: 10.2353/jmoldx.2010.090123. Epub 2010 Mar 4. J Mol Diagn. 2010. PMID: 20203005 Free PMC article.

10

Novel factor V C2-domain mutation (R2074H) in two families with factor V deficiency and bleeding.

Schrijver I, Houissa-Kastally R, Jones CD, Garcia KC, Zehnder JL. Schrijver I, et al. Thromb Haemost. 2002 Feb;87(2):294-9. Thromb Haemost. 2002. PMID: 11858490 Review.

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