Labor and cost requirements of two commercial assays for qualitative molecular detection of hepatitis C virusSCHRIJVER, Iris; BARON, Ellen Jo.Journal of clinical microbiology (Print). 2002, Vol 40, Num 9, pp 3476-3477, issn 0095-1137, 2 p.Article

Diagnostic single nucleotide polymorphism analysis of factor V Leiden and prothrombin 2021og>A: A comparison of the nanogen electronic microarray with restriction enzyme digestion and the Roche LightCyclerSCHRIJVER, Iris; LAY, Marla J; ZEHNDER, James L et al.American journal of clinical pathology. 2003, Vol 119, Num 4, pp 490-496, issn 0002-9173, 7 p.Article

Analysis of the Alternative Splicing of an FGFR2 Transcript Due to a Novel 5' Splice Site Mutation (1084+1 G>A): Case ReportTRAYNIS, Ilana; BERNSTEIN, Jonathan A; GARDNER, Phyllis et al.The Cleft palate-craniofacial journal. 2012, Vol 49, Num 1, pp 104-108, issn 1055-6656, 5 p.Article

Evaluation of a Gene Expression Microarray-based Assay to Determine Tissue Type of Origin on a Diverse Set of 49 MalignanciesBECK, Andrew H; RODRIGUEZ-PARIS, Juan; ZEHNDER, James et al.The American journal of surgical pathology. 2011, Vol 35, Num 7, pp 1030-1037, issn 0147-5185, 8 p.Article

A 30-month-old Child With Acute Renal Failure Due to Primary Renal Cytotoxic T-cell LymphomaPALADUGU, Srikanth; GARRO, Rouba; SCHRIJVER, Iris et al.The American journal of surgical pathology. 2010, Vol 34, Num 7, pp 1066-1070, issn 0147-5185, 5 p.Article

Novel contributions to the Asian CFTR mutation spectrum : Genotype and phenotype in Thai patients with cystic fibrosisSCHRIJVER, Iris; KARNSAKUL, Wikrom; LIMWONGSE, Chanin et al.American journal of medical genetics. 2005, Vol 133A, Num 1, pp 103-105, issn 0148-7299, 3 p.Article

T-cell clonality analysis in biopsy specimens from two different skin sites shows high specificity in the diagnosis of patients with suggested mycosis fungoidesTHURBER, Stacy E; BING ZHANG; KIM, Youn H et al.Journal of the American Academy of Dermatology. 2007, Vol 57, Num 5, pp 782-790, issn 0190-9622, 9 p.Article

Spontaneous spinal cerebrospinal fluid leaks and minor skeletal features of Marfan syndrome: a microfibrillopathySCHRIJVER, Iris; SCHIEVINK, Wouter I; GODFREY, Maurice et al.Journal of neurosurgery. 2002, Vol 96, Num 3, pp 483-489, issn 0022-3085Article

ACANTHOSIS NIGRICANS AND HYPOCHONDROPLASIA IN A CHILD WITH A K650Q MUTATION IN FGFR3BERK, David R; DEL CARMEN BOENTE, Maria; MONTANARI, Daniela et al.Pediatric dermatology. 2010, Vol 27, Num 6, pp 664-666, issn 0736-8046, 3 p.Article

Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray : A new approach for newborn screening follow-upGARDNER, Phyllis; OITMAA, Eneli; MESSNER, Anna et al.Pediatrics (Evanston). 2006, Vol 118, Num 3, pp 985-994, issn 0031-4005, 10 p.Article

Homozygous factor V splice site mutation associated with severe factor V deficiencySCHRIJVER, Iris; KOERPER, Marion A; JONES, Carol D et al.Blood. 2002, Vol 99, Num 8, pp 3063-3065, issn 0006-4971Article

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachGIARDINE, Belinda; BORG, Joseph; COSTA, Flavia C et al.Nature genetics. 2011, Vol 43, Num 4, pp 295-301, issn 1061-4036, 7 p.Article

Hereditary diffuse gastric cancer due to a previously undescribed CDH1 splice site mutationMATSUKUMA, Karen E; MULLINS, Franklin M; DIETZ, Lisa et al.Human pathology. 2010, Vol 41, Num 8, pp 1200-1203, issn 0046-8177, 4 p.Article

Microsatellite Instability and Mismatch Repair Protein Defects in Ovarian Epithelial Neoplasms in Patients 50 Years of Age and YoungerJENSEN, Kristin C; RAJAN MARIAPPAN, M; PUTCHA, Girish V et al.The American journal of surgical pathology. 2008, Vol 32, Num 7, pp 1029-1037, issn 0147-5185, 9 p.Article