98 results on '"Rabinowitz, Matthew"'
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52. Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci
53. Non-invasive detection of fetal aneuploidy across five chromosomes in the first trimester by targeted sequencing: P1-62
54. TESTICULAR ULTRASOUND AS A PROGNOSTIC FACTOR FOR IMPROVEMENT IN SEMEN PARAMETERS AFTER VARICOCELECTOMY
55. Resident involvement in the prostatic urethral lift: implementing innovative technology in an academic setting.
56. Accurate prediction of HIV-1 drug response from the reverse transcriptase and protease amino acid sequences using sparse models created by convex optimization
57. System using leo satellites for centimeter-level navigation
58. Method and system for training dynamic nonlinear adaptive filters which have embedded memory
59. Analysis of Plasma Cell-Free DNA by Ultradeep Sequencing in Patients With Stages I to III Colorectal Cancer
60. Abstract 913: Early detection of metastatic relapse and monitoring of therapeutic efficacy by ultra-deep sequencing of plasma cell-free DNA in patients with urothelial bladder carcinoma
61. Early Detection of Metastatic Relapse and Monitoring of Therapeutic Efficacy by Ultra-Deep Sequencing of Plasma Cell-Free DNA in Patients With Urothelial Bladder Carcinoma
62. Pregnancy outcomes from more than 1,800 in vitro fertilization cycles with the use of 24-chromosome single-nucleotide polymorphism–based preimplantation genetic testing for aneuploidy
63. Common variants associated with mitotic-origin of aneuploidy in human embryos
64. Erratum: Corrigendum: Phylogenetic ctDNA analysis depicts early-stage lung cancer evolution
65. Plenty of Food Aid Is Getting to Gaza.
66. Effects of maternal age on euploidy rates in a large cohort of embryos analyzed with 24-chromosome single-nucleotide polymorphism–based preimplantation genetic screening
67. Correction: Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics
68. Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development
69. Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a Massively Multiplexed PCR Methodology
70. Expanding the Scope of Noninvasive Prenatal Testing
71. An Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population
72. Common Variants Spanning PLK4 Are Associated With Mitotic-Origin Aneuploidy in Human Embryos
73. Abstract P4-02-03: Detection of single nucleotide variations and copy number variations in breast cancer tissue and ctDNA samples using single-nucleotide polymorphism-targeted massively multiplexed PCR
74. Whole genome prediction for preimplantation genetic diagnosis
75. Response to Drábek and Cereda
76. Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR
77. Non-invasive Cell-free Tumor DNA-based Detection of Breast Cancer-related Copy Number Variations
78. Non-Invasive Prenatal Detection of Trisomy 13 Using a Single Nucleotide Polymorphism- and Informatics-Based Approach
79. Noninvasive Aneuploidy Detection by Multiplexed Amplification and Sequencing of Polymorphic Loci
80. Noninvasive Cell-Free DNA-Based Prenatal Detection of Microdeletions Using Single Nucleotide Polymorphism–Targeted Sequencing
81. Beyond Compare: Online Retailer Assessed Multi-Million Civil Penalty In California For Allegedly Deceptive Price Comparisons
82. Informatics-based, highly accurate, noninvasive prenatal paternity testing
83. 591: Using targeted sequencing of SNPs to achieve a highly accurate non-invasive detection of fetal aneuploidy of 13, 18, 21 and sex chromosomes
84. Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics
85. Origins and rates of aneuploidy in human blastomeres
86. 715: A novel and highly accurate method for noninvasive prenatal diagnosis using parental genotypes
87. Non-invasive prenatal testing for whole chromosome abnormalities/Nicht invasives pränatales Testen auf Chromosomenstörungen
88. 714: A novel targeted sequencing approach improves noninvasive detection of chromosome ploidy in the first trimester
89. Accurate prediction of HIV-1 drug response from the reverse transcriptase and protease amino acid sequences using sparse models created by convex optimization
90. Augmenting GPS with Television Signals for Reliable Indoor Positioning
91. Abdominal Mass in a Phenotypic Female with 46,XY Differences in Sex Development.
92. Robustness of TOA and TDOA Positioning Under Suboptimal Weighting Conditions.
93. Correlation between variant allele frequency and mean tumor molecules with tumor burden in patients with solid tumors.
94. Foreign Supplier Verification.
95. Use of Polygenic Scores to Select Embryos.
96. Urethral bulking with native tissue during artificial urinary sphincter surgery.
97. Onset of azoospermia in man treated with ipilimumab/nivolumab for BRAF negative metastatic melanoma.
98. Patient Experience with Karyotyping After First Trimester Miscarriage: A National Survey.
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