Works matching DE "COMPARATIVE genomic hybridization"
Results: 1633
Advances in Understanding the Karyotype Evolution of Tetrapulmonata and Two Other Arachnid Taxa, Ricinulei and Solifugae.
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- Genes, 2025, v. 16, n. 2, p. 207, doi. 10.3390/genes16020207
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- Publication type:
- Article
Cytogenetics: Past, Present And Future.
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- Malaysian Journal of Medical Sciences, 2009, v. 16, n. 2, p. 4
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- Publication type:
- Article
Preliminary analysis of genomic abnormalities in canine meningiomas.
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- Veterinary & Comparative Oncology, 2008, v. 6, n. 3, p. 182, doi. 10.1111/j.1476-5829.2008.00159.x
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- Publication type:
- Article
Simultaneous Occurrences of Runs in Independent Markov Chains.
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- Methodology & Computing in Applied Probability, 2009, v. 11, n. 2, p. 267, doi. 10.1007/s11009-008-9093-3
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- Publication type:
- Article
Cytogenetic characterization of the Passiflora edulis Sims × Passiflora cincinnata Mast. interspecific hybrid and its parents.
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- Euphytica, 2016, v. 210, n. 1, p. 93, doi. 10.1007/s10681-016-1704-4
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- Publication type:
- Article
Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene.
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- Clinical & Experimental Nephrology, 2019, v. 23, n. 5, p. 669, doi. 10.1007/s10157-018-1682-z
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- Publication type:
- Article
Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases.
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- Clinical & Experimental Nephrology, 2018, v. 22, n. 4, p. 881, doi. 10.1007/s10157-018-1534-x
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- Publication type:
- Article
Computational detection and experimental validation of segmental duplications and associated copy number variations in water buffalo (Bubalus bubalis).
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- Functional & Integrative Genomics, 2019, v. 19, n. 3, p. 409, doi. 10.1007/s10142-019-00657-4
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- Publication type:
- Article
Comparative genomic hybridisation analysis of keloid tissue in Caucasians suggests possible involvement of HLA-DRB5 in disease pathogenesis.
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- Archives of Dermatological Research, 2012, v. 304, n. 3, p. 241, doi. 10.1007/s00403-011-1182-4
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- Article
Preservation of skin DNA for oligonucleotide array CGH studies: a feasibility study.
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- Archives of Dermatological Research, 2007, v. 299, n. 7, p. 353, doi. 10.1007/s00403-007-0773-6
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- Publication type:
- Article
Copia-like retrotransposons in the genus Setaria: Sequence heterogeneity, species distribution and chromosomal organization.
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- Plant Systematics & Evolution, 2003, v. 237, n. 3/4, p. 127, doi. 10.1007/s00606-002-0250-9
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- Publication type:
- Article
US variant porcine epidemic diarrhea virus: histological lesions and genetic characterization.
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- Virus Genes, 2016, v. 52, n. 4, p. 578, doi. 10.1007/s11262-016-1334-x
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- Publication type:
- Article
A Novel Molecular Cytogenetic Finding of Leiomyomatosis Peritonealis Disseminata.
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- Gynecologic & Obstetric Investigation, 2016, v. 81, n. 2, p. 186, doi. 10.1159/000381262
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- Publication type:
- Article
A Case of 46,X,der(X)t(X;X)(q22.1;p11) Xq22.1→Xqter in a 12-Year-Old Girl with Premature Ovarian Failure.
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- Gynecologic & Obstetric Investigation, 2007, v. 63, n. 3, p. 137, doi. 10.1159/000096436
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- Publication type:
- Article
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1.
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- Human Genetics, 2023, v. 142, n. 1, p. 1, doi. 10.1007/s00439-022-02476-3
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- Publication type:
- Article
Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant.
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- 2020
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- Publication type:
- Letter
Complex chromosomal rearrangements of human chromosome 21 in a patient manifesting clinical features partially overlapped with that of Down syndrome.
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- Human Genetics, 2020, v. 139, n. 12, p. 1555, doi. 10.1007/s00439-020-02196-6
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- Publication type:
- Article
Characterization and comparative genomic analysis of virulent and temperate Bacillus megaterium bacteriophages.
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- PeerJ, 2018, p. 1, doi. 10.7717/peerj.5687
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- Publication type:
- Article
Multi-Institutional Phase II Study of S-1 Monotherapy in Advanced Gastric Cancer with Pharmacokinetic and Pharmacogenomic Evaluations.
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- Oncologist, 2007, v. 12, n. 5, p. 543, doi. 10.1634/theoncologist.12-5-543
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- Publication type:
- Article
BAC Clones Related to Prognosis in Patients with Esophageal Squamous Carcinoma: An Array Comparative Genomic Hybridization Study.
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- Oncologist, 2007, v. 12, n. 4, p. 406, doi. 10.1634/theoncologist.12-4-406
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- Publication type:
- Article
New Insights into the Evolution of the W Chromosome in Lepidoptera.
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- Journal of Heredity, 2017, v. 108, n. 7, p. 709, doi. 10.1093/jhered/esx063
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- Publication type:
- Article
Mapping Genes to Chicken Microchromosome 16 and Discovery of Olfactory and Scavenger Receptor Genes Near the Major Histocompatibility Complex.
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- Journal of Heredity, 2014, v. 105, n. 2, p. 203, doi. 10.1093/jhered/est091
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- Publication type:
- Article
Erratum.
- Published in:
- 2007
- Publication type:
- Correction Notice
A Cytogenetically Characterized, Genome-Anchored 10-Mb BAC Set and CGH Array for the Domestic Dog.
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- Journal of Heredity, 2007, v. 98, n. 5, p. 474, doi. 10.1093/jhered/esm053
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- Publication type:
- Article
Genome-wide screening for genetic changes in a matched pair of benign and prostate cancer cell lines using array CGH.
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- Prostate Cancer & Prostatic Diseases, 2005, v. 8, n. 4, p. 335, doi. 10.1038/sj.pcan.4500826
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- Publication type:
- Article
Comparative Genomic In Situ Hybridization and the Possible Role of Retroelements in the Karyotypic Evolution of Three Akodontini Species.
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- International Journal of Genomics, 2017, p. 1, doi. 10.1155/2017/5935380
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- Publication type:
- Article
Microarray-Based Genomic Analysis Identifies Germline and Somatic Copy Number Variants and Loss of Heterozygosity in Acute Myeloid Leukaemia.
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- Malaysian Journal of Medicine & Health Sciences, 2018, v. 14, n. SP3, p. 11
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- Publication type:
- Article
Satellitome analysis on the pale-breasted thrush Turdus leucomelas (Passeriformes; Turdidae) uncovers the putative co-evolution of sex chromosomes and satellite DNAs.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-71635-5
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- Publication type:
- Article
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.
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- Brain Sciences (2076-3425), 2024, v. 14, n. 3, p. 273, doi. 10.3390/brainsci14030273
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- Publication type:
- Article
Comparative Genomic Hybridization (CGH) in New World Monkeys (Primates) Reveals the Distribution of Repetitive Sequences in Cebinae and Callitrichinae.
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- Biology (2079-7737), 2025, v. 14, n. 1, p. 22, doi. 10.3390/biology14010022
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- Publication type:
- Article
Intriguing link between fetal intracranial hemorrhage and X‐linked recessive chondrodysplasia punctata.
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- Ultrasound in Obstetrics & Gynecology, 2024, v. 64, n. 2, p. 259, doi. 10.1002/uog.27573
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- Publication type:
- Article
Late first‐trimester ultrasound findings can alter management after high‐risk NIPT result.
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- Ultrasound in Obstetrics & Gynecology, 2023, v. 62, n. 4, p. 497, doi. 10.1002/uog.26272
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- Publication type:
- Article
Non-invasive prenatal testing: what are we missing?
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- 2021
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- Publication type:
- Letter
ISUOG consensus statement on current understanding of the association of neurodevelopmental delay and congenital heart disease: impact on prenatal counseling.
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- 2017
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- Publication type:
- journal article
Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing.
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- Ultrasound in Obstetrics & Gynecology, 2015, v. 45, n. 4, p. 394, doi. 10.1002/uog.14767
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- Publication type:
- Article
Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 43, n. 4, p. 404, doi. 10.1002/uog.13236
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- Publication type:
- Article
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 43, n. 4, p. 396, doi. 10.1002/uog.12550
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- Publication type:
- Article
Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.
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- Ultrasound in Obstetrics & Gynecology, 2013, v. 41, n. 5, p. 500, doi. 10.1002/uog.12429
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- Publication type:
- Article
Re: Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.
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- 2013
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- Publication type:
- Opinion
Microarray comparative genomic hybridization in prenatal diagnosis: a review.
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- Ultrasound in Obstetrics & Gynecology, 2012, v. 40, n. 4, p. 385, doi. 10.1002/uog.11180
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- Publication type:
- Article
OC20.06: Whole-genome array CGH in fetuses with major malformations: a Danish study.
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- Ultrasound in Obstetrics & Gynecology, 2012, v. 40, p. 41, doi. 10.1002/uog.11352
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- Publication type:
- Article
Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
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- Ultrasound in Obstetrics & Gynecology, 2011, v. 38, n. 3, p. 314, doi. 10.1002/uog.8988
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- Publication type:
- Article
Array Comparative Genomic Hybridization Analysis Reveals Significantly Enriched Pathways in Canine Oral Melanoma.
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- Frontiers in Oncology, 2019, v. 9, p. 1, doi. 10.3389/fonc.2019.01397
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- Publication type:
- Article
B-ALL With t(5;14)(q31;q32); IGH-IL3 Rearrangement and Eosinophilia: A Comprehensive Analysis of a Peculiar IGH -Rearranged B-ALL.
- Published in:
- Frontiers in Oncology, 2019, v. 9, p. 1, doi. 10.3389/fonc.2019.01374
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- Publication type:
- Article
An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1472543
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- Publication type:
- Article
A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings.
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- Case Reports in Pathology, 2016, p. 1, doi. 10.1155/2016/1532424
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- Publication type:
- Article
Prenatal Lethal Diagnosis of 8p23.1 Duplication Syndrome Associated with Omphalocele and Encephalocele.
- Published in:
- 2023
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- Publication type:
- Case Study
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma.
- Published in:
- 2022
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- Publication type:
- Case Study
Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin.
- Published in:
- Case Reports in Genetics, 2020, p. 1, doi. 10.1155/2020/8897541
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- Publication type:
- Article
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis.
- Published in:
- 2017
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- Publication type:
- Case Study