Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities

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Items 301–400 of 468

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7. A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients with X-Linked Disorders
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14. Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH
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15. Parent-reported phenotype data on chromosome 6 aberrations collected via an online questionnaire: data consistency and data availability
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17. Using Microarray-based Molecular Cytogenetic Methods to Identify Chromosome Abnormalities
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18. Detection of single clone deletions using array CGH: Identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system
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22. A novel MBD5 mutation in an intellectually disabled adult female patient with epilepsy: Suggestive of early onset dementia?
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24. Array-based Comparative Genomic Hybridization and Its Application to Cancer Genomes and Human Genetics
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25. Overview of Cytogenetic Technologies
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26. Higher CNV Frequencies in Chromosome 14 of Girls With Turner Syndrome Phenotype
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28. High resolution array in the clinical approach to chromosomal phenotypes
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32. Genome-Wide Array Analysis Reveals Novel Genomic Regions and Candidate Gene for Intellectual Disability
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33. Clinical Genetics for the Dental Practitioner
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34. La CGH array : un bouleversement de la pratique hospitalière en cytogénétique
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36. Causes of Congenital Malformations
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37. L'hybridation génomique comparative sur microréseau d'ADN (puces à ADN) en pathologie chromosomique constitutionnelle
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38. Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA
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39. Integrated analysis revealing genome‑wide chromosomal copy number variation in supraglottic laryngeal squamous cell carcinoma
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40. Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array
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41. Diagnóstico prenatal y array-hibridación genómica comparada (CGH) (I). Gestaciones de elevado riesgo
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44. Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization.
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45. Faculty Opinions recommendation of Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
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46. Clinical Applications of Whole-Genome Chromosomal Microarray Analysis
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47. Array-Based Comparative Genomic Hybridization
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49. Gestion des variations du nombre de séquences génomiques (CNV) en génétique humaine constitutionnelle utilisant l’hybridation génomique comparative en microréseau d’ADN (HGCM)
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50. Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation
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51. THE APPLICATION OF MICROARRAY BASED COMPARATIVE GENOMIC HYBRIDIZATION IN PRENATAL DIAGNOSIS
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54. Chromosomal Microarray Analysis Uncovers Pathogenic Copy Number Variations in Unexplained Neurodevelopmental Disorders and Congenital Anomalies
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60. Diagnostic Genome Profiling in Mental Retardation
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61. Ladder-like amplification of the type I interferon gene cluster in the human osteosarcoma cell line MG63
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62. Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA
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64. Subtelomeric Rearrangements in Unexplained Mental Retardation
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94. Prenatal Diagnosis by Microarray Analysis
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