Found: 8
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Apparent Germline Mosaicism for a Novel 19p13.13 Deletion Disrupting NFIX and CACNA1A.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1105, doi. 10.1002/ajmg.a.35790
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- Article
2q24 deletions: Further characterization of clinical findings and their relation to the SCN cluster.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 11, p. 2767, doi. 10.1002/ajmg.a.35362
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- Article
An Eight-Gene Hypoxia Signature Predicts Survival in Pancreatic Cancer and Is Associated With an Immunosuppressed Tumor Microenvironment.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.680435
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- Article
Update of the International AGT Ambassador Program.
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- Journal of the Association of Genetic Technologists, 2023, v. 49, n. 4, p. 178
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- Article
A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 9, p. 2224, doi. 10.1002/ajmg.a.34120
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- Article
Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 2, p. 418, doi. 10.1002/ajmg.a.33827
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- Article
Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays.
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- Human Mutation, 2006, v. 27, n. 5, p. 467, doi. 10.1002/humu.20322
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- Article
A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 21, p. 2817, doi. 10.1093/hmg/ddg301
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- Article