Maria Soller (Former)
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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
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
Delection 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 area
(
- Contribution to journal › Article
- 2007
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Mark
Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer
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- Contribution to journal › Article
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Mark
Cytogenetic findings in pediatric renal cell carcinoma
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- Contribution to journal › Article
- 2006
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Mark
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.
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- Contribution to journal › Letter
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Mark
Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy
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- Contribution to journal › Article
- 2004
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Mark
A model for karyotypic evolution in testicular germ cell tumors.
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- Contribution to journal › Article
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Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
(
- Contribution to journal › Article
- 2003
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Mark
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors
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- Contribution to journal › Article