Found: 10
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Germ cell tumours in neonates and infants: a distinct subgroup?
- Published in:
- APMIS, 2003, v. 111, n. 1, p. 152, doi. 10.1034/j.1600-0463.2003.1110119_1.x
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- Article
Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome.
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- European Journal of Human Genetics, 2015, v. 23, n. 3, p. 317, doi. 10.1038/ejhg.2014.115
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- Article
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 936, doi. 10.1038/ejhg.2012.285
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- Article
Regulation of the MiTF/TFE bHLH‐LZ transcription factors through restricted spatial expression and alternative splicing of functional domains.
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- Nucleic Acids Research, 2004, v. 32, n. 8, p. 2315, doi. 10.1093/nar/gkh571
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- Article
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 1, p. 11, doi. 10.1002/gcc.22001
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- Article
Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21).
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 2, p. 107, doi. 10.1002/gcc.10243
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- Article
The cancer-related protein SSX2 interacts with the human homologue of a Ras-like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IP.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 3, p. 285, doi. 10.1002/gcc.10073
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- Article
A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 115, doi. 10.1002/(SICI)1098-2264(199910)26:2<115::AID-GCC3>3.0.CO;2-E
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- Article
Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndrome.
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- Human Mutation, 2011, v. 32, n. 7, p. 853, doi. 10.1002/humu.21523
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- Article
Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitution.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 14, p. 1661, doi. 10.1093/hmg/ddg178
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- Article