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- 2008
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Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
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- Contribution to journal › Article
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Mark
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
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- Contribution to journal › Article
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Mark
The hypermethylome of pediatric acute lymphoblastic leukemia
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- Contribution to journal › Published meeting abstract
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Mark
Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype-phenotype correlation and a comprehensive review of previously published cases.
(
- Contribution to journal › Article
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Mark
BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias.
(
- Contribution to journal › Article