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1.
Clinical validation of an array CGH test for HER2 status in breast cancer reveals that polysomy 17 is a rare event.
Mod Pathol
; 22(9): 1169-75, 2009 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-19448591
2.
Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia.
J Mol Diagn
; 10(5): 442-51, 2008 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-18687794
3.
Sequences in antibody molecules important for receptor-mediated transport into the chicken egg yolk.
Mol Immunol
; 38(8): 619-25, 2002 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-11792430
4.
Fluorescence in situ hybridization (FISH) for identifying the genomic rearrangements associated with three myelinopathies. Charcot-Marie-Tooth disease, hereditary neuropathy with liability to pressure palsies, and Pelizaeus-Merzbacher disease.
Methods Mol Biol
; 217: 219-38, 2003.
Artículo
en Inglés
| MEDLINE | ID: mdl-12491936
5.
Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene.
Leuk Res
; 33(9): 1276-81, 2009 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-19027161
6.
The HemeScan test for genomic prognostic marker assessment in chronic lymphocytic leukemia.
Expert Opin Med Diagn
; 2(6): 731-40, 2008 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23495782
7.
Comparative genomic hybridization arrays in clinical pathology: progress and challenges.
Mol Diagn Ther
; 11(2): 73-7, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-17397242
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