PCR screening for 22q11.2 microdeletion: Development of a new cost-effective diagnostic tool

Clinica Chimica Acta

Volumn 369, Issue 1, 2006, Pages 78-81

  Gioli Pereira, L ^a   Pereira, A C ^a   Mesquita, S M ^a   Lopes, A A ^a   Krieger, J E ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

22q11.2; Diagnostic; Microdeletion

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; FEMALE; GENE AMPLIFICATION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC SCREENING; GENOTYPE; HETEROZYGOSITY; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; MALE; NORMAL HUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SENSITIVITY AND SPECIFICITY; SINGLE NUCLEOTIDE POLYMORPHISM; VELOCARDIOFACIAL SYNDROME;

ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENETIC SCREENING; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33646889085     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2006.01.005     Document Type: Article

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