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Ethical questions concerning newborn genetic screening.
Esquerda M, Palau F, Lorenzo D, Cambra FJ, Bofarull M, Cusi V, Interdisciplinar En Bioetica G. Esquerda M, et al. Among authors: cusi v. Clin Genet. 2021 Jan;99(1):93-98. doi: 10.1111/cge.13828. Epub 2020 Sep 2. Clin Genet. 2021. PMID: 32779199 Review.
Schinzel-Giedion syndrome: report of two sibs.
Antich J, Manzanares R, Camarasa F, Krauel X, Vila J, Cusi V. Antich J, et al. Among authors: cusi v. Am J Med Genet. 1995 Oct 23;59(1):96-9. doi: 10.1002/ajmg.1320590119. Am J Med Genet. 1995. PMID: 8849020
Limb body wall complex: analysis of eight fetuses.
Cusí V, Torrents M, Vila J, Antich J, Carrera JM. Cusí V, et al. Birth Defects Orig Artic Ser. 1996;30(1):165-70. Birth Defects Orig Artic Ser. 1996. PMID: 9125325 No abstract available.
Neonatal erythroderma as a first manifestation of Menkes disease.
Galve J, Vicente A, González-Enseñat MA, Pérez-Dueñas B, Cusí V, Møller LB, Julià M, Domínguez A, Ferrando J. Galve J, et al. Among authors: cusi v. Pediatrics. 2012 Jul;130(1):e239-42. doi: 10.1542/peds.2011-1558. Epub 2012 Jun 18. Pediatrics. 2012. PMID: 22711717
52 results