Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
Titel:
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
Auteur:
Margraf, Rebecca L. VanSant-Webb, Chad Sant, David Carey, John Hanson, Heather D'Astous, Jacques Viskochil, Dave Stevenson, David A. Mao, Rong
Verschenen in:
The journal of molecular diagnostics
Paginering:
Jaargang 19 (2017) nr. 3 pagina's 7 p.
Jaar:
2017
Inhoud:
Uitgever:
American Society for Investigative Pathology and the Association for Molecular Pathology