M. Jama

发表

Sequencing of Exon 28 of von Willebrand Factor and Glycoprotein IB Genes to Identify Type 2B von Willebrand Disease and Platelet Type-Von Willebrand Disease

M. Jama, 2010 .

Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine

E. Lyon, M. Hindiyeh, Nisreen Rumman, 2015, PloS one.

Elderly female with a personal and family history of a bleeding disorder.

E. Lyon, G. Rodgers, K. Smock, 2015, Clinical chemistry.

A comprehensive Triple Repeat Primed PCR (TR-PCR) and a Long-Range PCR (LR-PCR) agarose-based assay for improved genotyping of GAA repeats in Friedreich's Ataxia.

P. Bayrak-Toydemir, R. Margraf, N. S. Reading, 2022, The Journal of molecular diagnostics : JMD.

A simple, high-throughput assay for Fragile X expanded alleles using triple repeat primed PCR and capillary electrophoresis.

E. Lyon, T. Laver, P. Yu, 2010, The Journal of molecular diagnostics : JMD.

Simultaneous amplification, detection, and analysis of common mutations in the galactose-1-phosphate uridyl transferase gene.

E. Lyon, R. Mao, Lesa M Nelson, 2007, The Journal of molecular diagnostics : JMD.

Long-range (17.7 kb) allele-specific polymerase chain reaction method for direct haplotyping of R117H and IVS-8 mutations of the cystic fibrosis transmembrane regulator gene.

E. Lyon, Christine Miller, G. Pont-Kingdon, 2004, The Journal of molecular diagnostics : JMD.

Diagnostic utility of microsatellite genotyping for molar pregnancy testing.

Larissa V Furtado, E. Lyon, S. Tripp, 2013, Archives of pathology & laboratory medicine.

Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.

R. Mao, Wei Tang, Lan-Szu Chou, 2006, Clinical chemistry.

A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electrophoresis.

P. Szankasi, D. Bahler, M. Jama, 2008, The Journal of molecular diagnostics : JMD.

Quadruplex genotyping of F5, F2, and MTHFR variants in a single closed tube by high-resolution amplicon melting.

K. Voelkerding, J. Durtschi, C. Wittwer, 2008, Clinical chemistry.

Triplet repeat primed PCR simplifies testing for Huntington disease.

E. Lyon, Christine Miller, A. Millson, 2013, The Journal of molecular diagnostics : JMD.

Identification of Mycobacterium spp. by Using a Commercial 16S Ribosomal DNA Sequencing Kit and Additional Sequencing Libraries

K. Carroll, J. Cloud, D. Hillyard, 2002, Journal of Clinical Microbiology.

Consensus characterization of 16 FMR1 reference materials: a consortium study.

Amit Phansalkar, Elaine Lyon, Monique A Johnson, 2008, The Journal of molecular diagnostics : JMD.

Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencing.

E. Lyon, J. Swensen, P. Bayrak-Toydemir, 2014, The Journal of molecular diagnostics : JMD.

EIF2AK4 Mutations in Patients Diagnosed With Pulmonary Arterial Hypertension

P. Bayrak-Toydemir, G. Elliott, M. Dodson, 2017, Chest.

Design, development, validation, and use of synthetic nucleic acid controls for diagnostic purposes and application to cystic fibrosis testing.

E. Lyon, B. Bejjani, T. Christensen, 2007, The Journal of molecular diagnostics : JMD.