Pages that link to "Q73271661"
Jump to navigation
Jump to search
The following pages link to Recurrent chromosome alterations in hepatocellular carcinoma detected by comparative genomic hybridization (Q73271661):
Displaying 6 items.
- Investigation of chromosomal aberrations in Egyptian hepatocellular carcinoma patients by fluorescence in situ hybridization (Q33350024) (← links)
- Molecular genetics of hepatocellular neoplasia. (Q33680701) (← links)
- Chromosomal abnormalities determined by comparative genomic hybridization are helpful in the diagnosis of atypical hepatocellular neoplasms (Q37055721) (← links)
- CHD1L: a novel oncogene (Q37597560) (← links)
- rs2267531, a promoter SNP within glypican-3 gene in the X chromosome, is associated with hepatocellular carcinoma in Egyptians (Q64069285) (← links)
- Chromosomal changes in fibrolamellar hepatocellular carcinoma detected by array comparative genomic hybridization (Q79819006) (← links)