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- 2019
-
Mark
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
(
- Contribution to journal › Article
- 2016
-
Mark
Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 2012
-
Mark
Homozygous deletions of CDKN2A are present in all dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukaemias and may be important for leukaemic transformation
(
- Contribution to journal › Letter
- 2011
-
Mark
Detection of human cytomegalovirus in medulloblastomas reveals a potential therapeutic target
(
- Contribution to journal › Article
- 2010
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Mark
Livslång uppföljning krävs vid medfödd missbildning.
(
- Contribution to journal › Scientific review
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Mark
First Report on Metastasizing Small Bowel Carcinoids in First-Degree Relatives in Three Generations
(
- Contribution to journal › Article
- 2008
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Mark
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding
(
- Contribution to journal › Article
- 2007
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Mark
Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida
(
- Contribution to journal › Article
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Mark
Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD)
(
- Contribution to journal › Article
- 2006
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Mark
Mantle cell lymphomas acquire increased expression of CCL4, CCL5 and 4-1BB-L implicated in cell survival
(
- Contribution to journal › Article
- 2001
-
Mark
Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping
(
- Contribution to journal › Article
-
Mark
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
(
- Contribution to journal › Article