A rapid and sensitive protocol for prenatal molecular diagnosis of X-linked adrenoleukodystrophy

Clinica Chimica Acta

Volumn 411, Issue 23-24, 2010, Pages 1992-1997

  Lan, Fenghua ^a   Wang, Zhihong ^a   Ke, Longfeng ^a   Xie, Haihua ^a   Huang, Lianghu ^a   Huang, Huijuan ^a   Tu, Xiangdong ^a   Zheng, Dezhu ^a   Zeng, Jian ^a   Li, Huizhong ^a   Xin, Na ^a   Yang, Bosheng ^a  

^a FUJIAN MEDICAL UNIVERSITY   (China)

Author keywords

ABCD1; Prenatal diagnosis; X linked adrenoleukodystrophy

Indexed keywords

ABC TRANSPORTER A1; GENOMIC DNA;

ADRENOLEUKODYSTROPHY; ADULT; AMNION FLUID; ARTICLE; BLOOD SAMPLING; CHINA; CLINICAL ARTICLE; CLINICAL PROTOCOL; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DIAGNOSTIC ACCURACY; DNA ISOLATION; DOT HYBRIDIZATION; FEMALE; FETUS; FETUS RISK; FRAMESHIFT MUTATION; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC RISK; GENOTYPE; HETEROZYGOTE DETECTION; HIGH RISK POPULATION; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NONSENSE MUTATION; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SENSITIVITY ANALYSIS; SHORT TANDEM REPEAT; UMBILICAL CORD BLOOD;

ADRENOLEUKODYSTROPHY; ADULT; DNA CONTAMINATION; FEMALE; FETUS; FOLLOW-UP STUDIES; GENOME, HUMAN; GENOTYPE; HUMANS; MALE; MOLECULAR DIAGNOSTIC TECHNIQUES; PREGNANCY; PRENATAL DIAGNOSIS; SENSITIVITY AND SPECIFICITY; TIME FACTORS;

EID: 77957749246     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2010.08.019     Document Type: Article

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