págs. 1-2
Population Carrier Screening for Spinal Muscular Atrophy: A Position Statement of the Association for Molecular Pathology
Narasimhan Nagan, Christine Curtis, Iris Schrijver, Kasinathan Muralidharan, Robert B. Wilson, Shuji Ogino
págs. 3-6
Laboratory Guidelines for Detection, Interpretation, and Reporting of Maternal Cell Contamination in Prenatal Analyses: A Report of the Association for Molecular Pathology
Iris Schrijver, Narasimhan Nagan, Nicole E. Faulkner, Christine Curtis
págs. 7-11
págs. 12-22
Nicole Stark, Thomas Winder, Kathrin Geiger, Axel Muendlein, Alois H. Lang, Heinz Drexel, Simone Geller Rhomberg
págs. 23-28
Multiplexed Methylation Profiles of Tumor Suppressor Genes in Bladder Cancer
Esteban Orenes, Miguel Álvarez, Ana Blanca, Oscar Heredero, Alberto Palacios, Manuel Urrutia Avisrror, Jesús María Fernández, Antonio López Beltrán, Marta Sánchez Carbayo, Maria José Cabello, Laura Grau, Noreli Franco
págs. 29-40
Establishment of a Molecular Diagnostic System for Spinal Muscular Atrophy: Experience From a Clinical Laboratory in China
Aizhen Yan, Yanhong Lin, Jian Zeng, Fenghua Lan, Zhongyong Zhu, Longfeng Ke
págs. 41-47
J. Scott Nystrom, C. Te Rigl, Rebecca Deeter, Raji Pillai, W. David Henner, Ljubomir Buturovic, Meredith Halks Miller
págs. 48-56
págs. 57-63
Detection of KRAS and BRAF Mutations in Colorectal Carcinoma: Roles for High-Sensitivity Locked Nucleic Acid-PCR Sequencing and Broad-Spectrum Mass Spectrometry Genotyping
págs. 64-73
Pierre P. Massion, Christine H Chung, Darrell R. Borger, Ya Lun Lin, Katherine Hutchinson, MarKeesa Duke, Dora Dias Santagata, Zengliu Su, William Pao, A. John Lafrate, Cindy L. Vnencak Jones
págs. 74-84
PCR, A Simple Method to Detect Translocations and Insertion/Deletion Mutations
Michael J. Hafez, Shuko Harada, Kathleen M. Murphy, James R. Eshleman, Christopher D. Gocke, Ming Tseh Lin, Li Hui Tseng , Roy G. Rich
págs. 85-92
Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases
Stephen N. Thibodeau, Brittany C. Thomas, Kara A. Mensink, Steven Gallinger, Spring Holter, Polly A. Newcomb, John D. Potter, Mark A. Jenkins, Tiffany Long, Daniel J. Weisenberger, Robert W. Haile, Graham Casey, Kandelaria Rumilla, Peter W. Laird, Karen V. Schowalter, Loic Le Marchand, Noralane M. Lindor
págs. 93-99
Sanna Ranghia Santhosh, Vasanthapuram Ravi, Reeta Mani, Maria Thomas, Shashi Khare, Arvind Rai, Radha Kant Ratho, Sujit Pujari, Bijayanti Mishra, Venkata Lakshmana , Rao Putcha , Rajagopalan Vijayaraghavan, Manmohan Parida, Jyoti Shukla, Shashi Sharma
págs. 100-107
Allelic Dropout Can Cause False-Positive Results for Prader-Willi and Angelman Syndrome Testing
Syed Hussain Askree, Lora J. H. Bean, Madhuri Hedge, Bradford Coffee, Margaret Adam, Muhammad Ali Pervaiz, Lawrence N. Hjelm
págs. 108-112
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