Preimplantation genetic diagnosis for cystic fibrosis: a case report

Autor: Biazotti, Maria Cristina Santoro, Pinto Junior, Walter, Albuquerque, Maria Cecília Romano Maciel de, Fujihara, Litsuko Shimabukuro, Suganuma, Cláudia Haru, Reigota, Renata Bednar, Bertuzzo, Carmen Sílvia

Publikováno v: einstein (São Paulo) v.13 n.1 2015
Einstein (São Paulo)
Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron:IIEPAE
Einstein (São Paulo), Volume: 13, Issue: 1, Pages: 110-113, Published: MAR 2015

Cystic fibrosis is an autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator gene. This disorder produces a variable phenotype including lung disease, pancreatic insufficiency, and meconium ileus p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fb64440e34d448da85d19c6834dab3bb
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082015000100019