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DISCUSSION.
- Published in:
- Journal of Finance (Wiley-Blackwell), 1973, v. 28, n. 2, p. 369, doi. 10.2307/2978309
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- Article
Detection of copy number changes at the NF1 locus with improved high-resolution array CGH.
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- Clinical Genetics, 2007, v. 72, n. 3, p. 238, doi. 10.1111/j.1399-0004.2007.00858.x
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- Article
Replication study implicates COMT val158met polymorphism as a modulator of probabilistic reward learning.
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- Genes, Brain & Behavior, 2015, v. 14, n. 6, p. 486, doi. 10.1111/gbb.12228
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- Article
Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection.
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- Journal of Molecular Medicine, 2003, v. 81, n. 7, p. 443, doi. 10.1007/s00109-003-0458-3
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- Article
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls.
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- Translational Psychiatry, 2017, v. 7, n. 1, p. e1012, doi. 10.1038/tp.2016.286
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- Article
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
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- International Journal of Cancer, 2006, v. 118, n. 5, p. 1159, doi. 10.1002/ijc.21385
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- Article
Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array.
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- Genes, Chromosomes & Cancer, 2009, v. 48, n. 10, p. 897, doi. 10.1002/gcc.20695
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- Article
Telomerase activity is a biomarker for high grade malignant peripheral nerve sheath tumors in neurofibromatosis type 1 individuals.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 3, p. 238, doi. 10.1002/gcc.20525
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- Article
Chromosome 22 tiling‐path array–CGH analysis identifies germ‐line‐ and tumor‐specific aberrations in patients with glioblastoma multiforme.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 161
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- Article
Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 4, p. 329, doi. 10.1002/gcc.20207
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- Article
High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas.
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- Genes, Chromosomes & Cancer, 2005, v. 42, n. 3, p. 228
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- Article
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs).
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- Human Mutation, 2008, v. 29, n. 1, p. 74, doi. 10.1002/humu.20601
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- Article
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.
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- Human Mutation, 2005, v. 26, n. 6, p. 540, doi. 10.1002/humu.20255
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- Article
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
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- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1497
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- Article
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
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- Human Molecular Genetics, 2002, v. 11, n. 25, p. 3221, doi. 10.1093/hmg/11.25.3221
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- Article