Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities

Genetic Testing

Volumn 11, Issue 4, 2007, Pages 467-475

  Bittel, Douglas C ^a   Kibiryeva, Nataliya ^a   Butler, Merlin G ^a,b  

^a UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

^b CHILDREN S MERCY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALGORITHM; ARTICLE; CHILD; CHROMOSOME 15 ABNORMALITY; CHROMOSOME 15Q; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; DIAGNOSTIC ACCURACY; DIAGNOSTIC KIT; DIAGNOSTIC VALUE; DNA METHYLATION; EVALUATION; FEMALE; GENE AMPLIFICATION; GENE DELETION; GENOME IMPRINTING; GENOTYPE; HAPPY PUPPET SYNDROME; HUMAN; INFANT; MALE; METHYLATION SPECIFIC MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION ANALYSIS; PRADER WILLI SYNDROME;

ADOLESCENT; ADULT; ALGORITHMS; ANGELMAN SYNDROME; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; DNA METHYLATION; FEMALE; GENE DOSAGE; HUMANS; INFANT; MALE; NUCLEIC ACID AMPLIFICATION TECHNIQUES; NUCLEIC ACID PROBES; PRADER-WILLI SYNDROME;

EID: 38149068398     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/gte.2007.0061     Document Type: Article

References (20)

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