Cell-free fetal DNA screening for detection of microdeletion syndromes: A cost-effectiveness analysis. Avram Carmen M et al. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2019 Jul 1-251

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Last Posted: Jul 25, 2019

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• Cell-free fetal DNA screening for detection of microdeletion syndromes: A cost-effectiveness analysis.
  Avram Carmen M et al. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2019 Jul 1-251
• Genomic profiling of blood-derived circulating tumor DNA from patients with colorectal cancer: Implications for response and resistance to targeted therapeutics.
  Choi In Sil et al. Molecular cancer therapeutics 2019 Jul
• What is the role of next generation sequencing in status epilepticus?
  Guerrini Renzo et al. Epilepsy & behavior : E&B 2019 Jul
• Genetic Susceptibility to Chronic Kidney Disease - Some More Pieces for the Heritability Puzzle.
  Cañadas-Garre Marisa et al. Frontiers in genetics 2019 10453
• Additive Diagnostic Yield of Homozygosity Regions Identified During Chromosomal microarray Testing in Children with Developmental Delay, Dysmorphic Features or Congenital Anomalies.
  Ali Mohamed A M et al. Biochemical genetics 2019 Jul
• Rare germline copy number variants in colorectal cancer predisposition characterized by exome sequencing analysis.
  Franch-Expósito Sebastià et al. Journal of genetics and genomics = Yi chuan xue bao 2018 45(1) 41-45
• Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
  Chau Matthew Hoi Kin et al. American journal of obstetrics and gynecology 2019 Jun
• Comprehensive mutation detection of BRCA1/2 genes reveals large genomic rearrangements contribute to hereditary breast and ovarian cancer in Chinese women.
  Cao Wen-Ming et al. BMC cancer 2019 Jun 19(1) 551
• A comparison of genomic laboratory reports and observations that may enhance their clinical utility for providers and patients.
  Davis Kyle Walter et al. Molecular genetics & genomic medicine 2019 May e551
• Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.
  Dharmadhikari Avinash V, et al. Genome medicine 2019 5 0. (1) 30

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