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Autor:
Bruna Cristina Longo, Rafael Chimiloski Turcatto, Ana Lúcia Carrinho Ayroza Rangel, Elaine Manoela Porto Amorin, Denise Cesar de Oliveira Davidoff, Adriano Tomio Hoshi, Maria de Fátima Tomasin, Francielle Carneiro Hirata, Maria Daniela Basso de Souza
Publikováno v:
ARCHIVES OF HEALTH INVESTIGATION. 11:907-911
Beckwith-Wiedemann Syndrome (BWS) is characterized by a disorder on chromosome 11p15, whose loci have growth-regulating genes. Among the numerous clinical features such anterior abdominal wall defects, omphalocele and genital abnormalities, the most