Found: 7
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Subcortical heterotopia appearing as huge midline mass in the newborn brain.
- Published in:
- Child's Nervous System, 2016, v. 32, n. 2, p. 377, doi. 10.1007/s00381-015-2841-0
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- Article
Compound heterozygous GFM2 mutations with Leigh syndrome complicated by arthrogryposis multiplex congenita.
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- Journal of Human Genetics, 2015, v. 60, n. 9, p. 509, doi. 10.1038/jhg.2015.57
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- Article
Allelic loss of chromosome 13q14.3 in human oral cancer: Correlation with lymph node metastasis.
- Published in:
- International Journal of Cancer, 1998, v. 79, n. 4, p. 312, doi. 10.1002/(SICI)1097-0215(19980821)79:4<312::AID-IJC2>3.0.CO;2-Y
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- Article
Localization of a tumour-suppressor gene associated with human oral cancer on 7q31.1.
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- International Journal of Cancer, 1998, v. 75, n. 5, p. 671, doi. 10.1002/(SICI)1097-0215(19980302)75:5<671::AID-IJC2>3.0.CO;2-W
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- Article
The role of common gamma chain in human monocytes in vivo ; evaluation from the studies of X-linked severe combined immunodeficiency (X-SCID) carriers and X-SCID patients who underwent cord blood stem cell transplantation.
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- British Journal of Haematology, 2002, v. 118, n. 3, p. 858, doi. 10.1046/j.1365-2141.2002.03679.x
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- Article
STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.
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- Epilepsia (Series 4), 2010, v. 51, n. 12, p. 2397, doi. 10.1111/j.1528-1167.2010.02728.x
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- Article
Everolimus Treatment for an Early Infantile Subependymal Giant Cell Astrocytoma With Tuberous Sclerosis Complex.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 9, p. 1192, doi. 10.1177/0883073814544703
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- Article