遺伝症候群と遺伝子治療のジャーナル | 7

Stefano Vicari, Floriana Costanzo, Marco Armando, Giovanni Carbonara, Pamela Varvara, Cristina Caciolo, Chiara Gagliardi, Tiziana Gianesini, Paolo Alfieri, Rossella Capolino and Deny Menghini

この記事をシェアする

研究論文

Hepatoblastoma and microRNA-483 Two Forms and One Outcome

Marco Salvatore, Armando Magrelli, Valentini Flamini, Andrea Brunati, Eleonora Basso, Renato Romagnoli, Ezio David and Domenica Taruscio

この記事をシェアする

研究論文

Easychip 8x15k: A New Tool for Detecting Chromosome Anomalies in Low Risk Pregnancies, Supporting and Integrating Standard Karyotype

Viola Alesi, Laura Bernardini, Didier Goidin, Michela Canestrelli, Maria Lisa Dentici, Giuseppe Barrano, Maria Grazia Giuffrida, Anna Maria Nardone, Diana Postorivo, Luigi Laino, Rita Genesio, Bruno Dallapiccola and Antonio Novelli

この記事をシェアする

遺伝症候群と遺伝子治療のジャーナル
オープンアクセス

音量 7, 問題 1 (2016)

Report: Fourth International Workshop for Glycosylation Defects in Muscular Dystrophies

Association of Superoxide Dismutase 2 Polymorphism Rs4880 and Open-Angle Glaucoma in a Greek Patients Cohort

Natural Compounds as Therapeutic Agents in the Treatment Cystic Fibrosis

Two Familial Cases of Robertsonian Transloacations 13; 14 and Its Clinical Consequences

Normal Child by a Gestational Carrier of a Phenylketonuria (PKU) Mother-An Alternative to Diet

Polyposis Caused by Low APC Mosaicism

Cytogenetic Study of Down Syndrome In Algeria: Report and Review

Detecting Psychiatric Profile in Genetic Syndromes: A Comparison of Down Syndrome and Williams Syndrome

Hepatoblastoma and microRNA-483 Two Forms and One Outcome

Easychip 8x15k: A New Tool for Detecting Chromosome Anomalies in Low Risk Pregnancies, Supporting and Integrating Standard Karyotype

遺伝症候群と遺伝子治療のジャーナルオープンアクセス

音量 7, 問題 1 (2016)

遺伝症候群と遺伝子治療のジャーナル
オープンアクセス