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CLINICAL SCIENCE
Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers
Roberta Lelis DutraI,II,
Corresponding author
roberta.dutra@icr.usp.br

Tel.: 55 11 30698671
, Patrícia de Campos PieriII, Ana Carolina Dias TeixeiraII, Rachel Sayuri HonjoI, Debora Romeo BertolaI, Chong Ae KimI
I Unidade de Genética Clínica, Instituto da Criança, Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
II Laboratório de Investigação em Pediatria Clínica - LIM-36, Instituto da Criança, Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
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ISSN: 18075932
Original language: English
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