Found: 15
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Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder.
- Published in:
- 2019
- By:
- Publication type:
- letter
Genome reduction and potential metabolic complementation of the dual endosymbionts in the whitefly Bemisia tabaci.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1379-6
- By:
- Publication type:
- Article
Genome reduction and potential metabolic complementation of the dual endosymbionts in the whitefly Bemisia tabaci
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 226, doi. 10.1186/s12864-015-1379-6
- By:
- Publication type:
- Article
Alpha Satellite Insertion Close to an Ancestral Centromeric Region.
- Published in:
- Molecular Biology & Evolution, 2021, v. 38, n. 12, p. 5576, doi. 10.1093/molbev/msab244
- By:
- Publication type:
- Article
Complete characterisation of two new large Xq28 duplications involving F8 using whole genome sequencing in patients without haemophilia A.
- Published in:
- Haemophilia, 2022, v. 28, n. 1, p. 117, doi. 10.1111/hae.14402
- By:
- Publication type:
- Article
Two Host Clades, Two Bacterial Arsenals: Evolution through Gene Losses in Facultative Endosymbionts.
- Published in:
- Genome Biology & Evolution, 2015, v. 7, n. 3, p. 839, doi. 10.1093/gbe/evv030
- By:
- Publication type:
- Article
The Genome of Cardinium cBtQ1 Provides Insights into Genome Reduction, Symbiont Motility, and Its Settlement in Bemisia tabaci.
- Published in:
- Genome Biology & Evolution, 2014, v. 6, n. 4, p. 1013, doi. 10.1093/gbe/evu077
- By:
- Publication type:
- Article
Supravalvular Aortic Stenosis Caused by a Familial Chromosome 7 Inversion Disrupting the ELN Gene Uncovered by Whole-Genome Sequencing.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 4, p. 209, doi. 10.1159/000500215
- By:
- Publication type:
- Article
Familial transmission of chromoanagenesis leads to unpredictable unbalanced rearrangements through meiotic recombination.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 4, p. 401, doi. 10.1111/cge.14291
- By:
- Publication type:
- Article
Development of a new expanded next‐generation sequencing panel for genetic diseases involved in dyslipidemia.
- Published in:
- Clinical Genetics, 2020, v. 98, n. 6, p. 589, doi. 10.1111/cge.13832
- By:
- Publication type:
- Article
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
- Published in:
- BMC Medical Genomics, 2018, v. 11, p. 1, doi. 10.1186/s12920-018-0338-x
- By:
- Publication type:
- Article
Whole Sequencing of Most Prevalent Dilated Cardiomyopathy-Causing Genes as a Molecular Strategy to Improve Molecular Diagnosis Efficiency?
- Published in:
- DNA & Cell Biology, 2021, v. 40, n. 3, p. 491, doi. 10.1089/dna.2020.6305
- By:
- Publication type:
- Article
Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy.
- Published in:
- Human Mutation, 2020, v. 41, n. 2, p. 465, doi. 10.1002/humu.23944
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- Publication type:
- Article
Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosis.
- Published in:
- Human Mutation, 2019, v. 40, n. 11, p. 1993, doi. 10.1002/humu.23845
- By:
- Publication type:
- Article
Genome sequencing in cytogenetics: Comparison of short‐read and linked‐read approaches for germline structural variant detection and characterization.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 3, p. 1, doi. 10.1002/mgg3.1114
- By:
- Publication type:
- Article