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Keyword [NICCD]
Result: 1 - 11 | Page: 1 of 1
1.
The Clinical Value Of The Galactitol Concentration In Urine Filter Paper Analyzed By GC/MS In Screening NICCD Patients
2.
The Significance Of SLC25A13 Gene Mutation In Chinese Infants With Intrahepatic Cholestasis
3.
SLC25A13 Gene Mutation Analyzed By PCR-reverse Dot-blotting Hybridization Method
4.
Mutation Spectrum And Clinical Features In Infants With Intrahepatic Cholestasis Caused By Citrin Deficiency
5.
Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency: Clinical Value Of Dynamic Alterations In Biochemical Markers
6.
Correlation Analysis Of SLC25A13Genotype And Biochemical Phenotype, And Serum Ceruloplasmin Levels And The Other Biochemical Alterations In NICCD Patient
7.
Identification Of The Novel Mutation IVS4ins6kb And Its Application In The Molecular Diagnosis Of NICCD Patients: Based On CDNA Cloning Analysis Of SLC25A13Gene In Peripheral Blood Lymphocytes
8.
Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency(NICCD): Clinical, Genetic And Functional Analysis Of A Family
9.
Gene And Clinicalanalysis Of Neonatal Intrahepatic Cholestasis Caused By Citrin Defciency(NICCD)
10.
Analysis Of Clinical Characteristics Of 709 Cases With Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency
11.
Comparative Study Of Sodium Taurocholate Cotransporting Polypeptide Deficiency And Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency
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