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Keyword [SLC25A13]
Result: 1 - 11 | Page: 1 of 1
1.
Construction And Analysis Of HCC Gene Expression Profile And High Resolution Map Of Abnormal Alterations In HCC Genomic DNA
2.
Analysis Of Regional Characteristics And Death Cases Of Intrahepatic Cholestasis In Infants Caused By Citrin Defects
3.
The Significance Of SLC25A13 Gene Mutation In Chinese Infants With Intrahepatic Cholestasis
4.
SLC25A13 Gene Mutation Analyzed By PCR-reverse Dot-blotting Hybridization Method
5.
Mutation Spectrum And Clinical Features In Infants With Intrahepatic Cholestasis Caused By Citrin Deficiency
6.
Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency: Clinical Value Of Dynamic Alterations In Biochemical Markers
7.
A Study About Establishing The Genetic Test Platform For Citrin Deficiency Based On Targeted Sequence Capture And High-throughput Sequencing And Its Clinical Applications
8.
Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency(NICCD): Clinical, Genetic And Functional Analysis Of A Family
9.
Molecular Diagnosis Of Pediatric Patients With Citrin Deficiency In China:SLC25A13 Mutation Spectrum And The Geographic Distribution
10.
Molecular Diagnostic And Clinical Phenotypic Analysis Of Citrin Deficiency
11.
Mitochondrial Carrier SLC25A13 Regulates Breast Cancer Cell Cycle
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