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1دورية أكاديمية
المؤلفون: Favaro, Francine P., Alvizi, Lucas, Zechi Ceide, Roseli M., Bertola, Debora, Felix, Temis M., de Souza, Josiane, Raskin, Salmo, Twigg, Stephen R. F., Weiner, Andrea Maria Julia, Armas, Pablo, Margarit, Ezequiel, Calcaterra, Nora Beatriz, Andersen, Gregers R., McGowan, Simon J., Wilkie, Andrew O. M., Richieri Costa, Antonio, de Almeida, Maria L. G., Passos Bueno, Maria Rita
مصطلحات موضوعية: Noncoding Expansion, Richieri-Costa-Pereira Syndrome, Craniofacial Disorder, Limb Defects, https://purl.org/becyt/ford/3.1Test, https://purl.org/becyt/ford/3Test
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0002929713005351Test; http://hdl.handle.net/11336/8819Test; Favaro, Francine P.; Alvizi, Lucas; Zechi Ceide, Roseli M.; Bertola, Debora; Felix, Temis M.; et al.; A Noncoding Expansion in EIF4A3 Causes Richieri-Costa-Pereira Syndrome, a Craniofacial Disorder Associated with Limb Defects; Cell Press; American Journal Of Human Genetics; 94; 1; 1-2014; 120-128
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2دورية أكاديمية
المؤلفون: Favaro, Francine P., Alvizi, Lucas, Zechi Ceide, Roseli M., Bertola, Debora, Felix, Temis M., de Souza, Josiane, Raskin, Salmo, Twigg, Stephen R. F., Weiner, Andrea Maria Julia, Armas, Pablo, Margarit, Ezequiel, Calcaterra, Nora Beatriz, Andersen, Gregers R., McGowan, Simon, Wilkie, Andrew O. M., Richieri Costa, Antonio, de Almeida, Maria L. G., Passos Bueno, Maria Rita
مصطلحات موضوعية: Richieri-Costa-Pereira Syndrome, Eif4a3, Craniofacial Disorder, https://purl.org/becyt/ford/3.1Test, https://purl.org/becyt/ford/3Test
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0002929713005351Test; http://hdl.handle.net/11336/29690Test; Favaro, Francine P.; Alvizi, Lucas; Zechi Ceide, Roseli M.; Bertola, Debora; Felix, Temis M.; et al.; A non-coding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects; Cell Press; American Journal Of Human Genetics; 94; 1; 1-2014; 120-128; CONICET Digital; CONICET