SCOPUS 정보 검색 플랫폼

Volumn 6, Issue 2, 2002, Pages 135-139

Simple fluorescent PCR assay for discriminating FRAXA fully mutated females from normal homozygotes

(8) Houdayer, Claude a Lourdaux, Julie a Billette De Villemeur, Thierry a Royer Legrain, Ghislaine b Bahuau, Michel a Bonnefont, Jean Paul b Feldmann, Delphine a Couderc, Rémy a

a ARMAND TROUSSEAU HOSPITAL (France)

b HÔPITAL NECKER ENFANTS MALADES (France)

Author keywords

[No Author keywords available]

Indexed keywords

PRIMER DNA;

ARTICLE; CHILD; COMPARATIVE STUDY; EXON; FEMALE; FRAGILE X SYNDROME; GENETICS; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMAN; MALE; MENTAL DEFICIENCY; METHODOLOGY; MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; REFERENCE VALUE; REPRODUCIBILITY; TRINUCLEOTIDE REPEAT; X CHROMOSOME; ALLELE; CLINICAL ARTICLE; CLINICAL PRACTICE; CONTROLLED STUDY; DIAGNOSTIC APPROACH ROUTE; DNA DETERMINATION; FLUORESCENCE; FMR1 GENE; FRAXA GENE; GENE AMPLIFICATION; GENE ISOLATION; GENE LOCUS; GENE MUTATION; HOMOZYGOSITY; HUMAN CELL; QUANTITATIVE GENETICS; RELIABILITY; SOUTHERN BLOTTING; SYNDROME DELINEATION; WILD TYPE;

BASE SEQUENCE; CHILD; CHROMOSOMES, HUMAN, X; DNA PRIMERS; EXONS; FEMALE; FRAGILE X SYNDROME; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; MALE; MENTAL RETARDATION; MUTATION; POLYMERASE CHAIN REACTION; REFERENCE VALUES; REPRODUCIBILITY OF RESULTS; TRINUCLEOTIDE REPEATS; COMPARATIVE STUDY; HUMAN; X CHROMOSOME;

EID: 0036591556 PISSN: 10906576 EISSN: None Source Type: Journal
DOI: 10.1089/10906570260199410 Document Type: Article

Times cited : (7)

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