oligonucleotide chromosomal microarray (GeneDx Inc)
90
Structured Review
GeneDx Inc
oligonucleotide chromosomal microarray
Oligonucleotide Chromosomal Microarray, supplied by GeneDx Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/clinical+chromosomal+microarray+database/chromosomal+microarray/pmc04731023-142-12-20
Average 90 stars, based on 1 article reviews
Oligonucleotide Chromosomal Microarray, supplied by GeneDx Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/clinical+chromosomal+microarray+database/chromosomal+microarray/pmc04731023-142-12-20
Average 90 stars, based on 1 article reviews
oligonucleotide chromosomal microarray - by Bioz Stars,
2026-09
90/100 stars
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Related Articles
Microarray:Article Title: Intracranial venous malformation masquerading as a meningioma in PI3KCA-related overgrowth spectrum disorder. Article Snippet: Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA Division of Neurosurgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA Department of Neurosurgery, Boston Medical Center, Boston University Medical School, Boston, Massachusetts, USA Department of Pathology, Boston Children's Hospital, Boston, Massachusetts, USA Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA Department of Radiology, Boston Children's Hospital, Boston, Massachusetts, USA Article Title: Expanding the genetic landscape of oral‐facial‐digital syndrome with two novel genes Article Snippet: Trio exome sequencing was performed on DNA from Patient 1 at GeneDx. .. Article Title: P776: Autosomal recessive cutis laxa type 1B in two successive pregnancies due to a novel homozygous EFEMP2 variant Article Snippet: .. The patient elected to pursue amniocentesis for Article Title: P775: Maternally inherited 11p15 duplication involving only part of the ICR1 H19/IGF2 domain: Unraveling mild Russell-Silver syndrome phenotype Article Snippet: .. The patient elected to pursue amniocentesis for Article Title: Behavioral variant frontotemporal dementia in a 23-year-old man. Article Snippet: .. Because chromosomal copy number variants (CNV) are enriched in patient populations with schizophrenia (Marshall et al., 2017; Raznahan et al., 2022), an Article Title: Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease Article Snippet: .. Biochemical testing revealed normal serum creatine kinase (CK) with a slight elevation of serum troponin T. Genetic testing included normal SCN5A sequencing, Article Title: Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. Article Snippet: Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA The Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Division of Nephrology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Boston, Massachusetts, USA Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Article Title: Expanding the KIF4A ‐associated phenotype Article Snippet: .. Other genetic findings , Sequencing:Article Title: Intracranial venous malformation masquerading as a meningioma in PI3KCA-related overgrowth spectrum disorder. Article Snippet: Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA Division of Neurosurgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA Department of Neurosurgery, Boston Medical Center, Boston University Medical School, Boston, Massachusetts, USA Department of Pathology, Boston Children's Hospital, Boston, Massachusetts, USA Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA Department of Radiology, Boston Children's Hospital, Boston, Massachusetts, USA Article Title: Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease Article Snippet: .. Biochemical testing revealed normal serum creatine kinase (CK) with a slight elevation of serum troponin T. Genetic testing included normal SCN5A sequencing, Article Title: Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. Article Snippet: Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA The Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Division of Nephrology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Boston, Massachusetts, USA Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Variant Assay:Article Title: Intracranial venous malformation masquerading as a meningioma in PI3KCA-related overgrowth spectrum disorder. Article Snippet: Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA Division of Neurosurgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA Department of Neurosurgery, Boston Medical Center, Boston University Medical School, Boston, Massachusetts, USA Department of Pathology, Boston Children's Hospital, Boston, Massachusetts, USA Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA Department of Radiology, Boston Children's Hospital, Boston, Massachusetts, USA Article Title: Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. Article Snippet: Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA The Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Division of Nephrology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Boston, Massachusetts, USA Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Biomarker Discovery:Article Title: Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. Article Snippet: Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA The Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Division of Nephrology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Boston, Massachusetts, USA Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA Methylation:Article Title: Expanding the KIF4A ‐associated phenotype Article Snippet: .. Other genetic findings , |