Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers

Clinics

Volumn 66, Issue 6, 2011, Pages 959-964

  Dutra, Roberta Lelis ^a   Pieri, Patrícia de Campos ^a   Teixeira, Ana Carolina Dias ^a   Honjo, Rachel Sayuri ^a   Bertola, Debora Romeo ^a   Kim, Chong Ae ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Microsatellite markers; Molecular diagnosis; Parental origin; Size deletion; Williams beuren syndrome

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 7; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC POLYMORPHISM; GENETICS; HUMAN; INFANT; MALE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; REPRODUCIBILITY; WILLIAMS BEUREN SYNDROME;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 7; FEMALE; GENE DELETION; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; REPRODUCIBILITY OF RESULTS; WILLIAMS SYNDROME;

EID: 79961155591     PISSN: 18075932     EISSN: None     Source Type: Journal    
DOI: 10.1590/S1807-59322011000600007     Document Type: Article

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