检索结果 - M Sorcini
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A Population-Based Study on the Frequency of Additional Congenital Malformations in Infants with Congenital Hypothyroidism: Data from the Italian Registry for Congenital Hypothyroi... 由 Antonella Olivieri, Maria A. Stazi, P Mastroiacovo, Cristina Fazzini, Emanuela Medda, A Spagnolo, Simona De Angelis, M. E. Grandolfo, Domenica Taruscio, Viviana Cordeddu, M Sorcini
出版 2002Artigo -
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Somatic <i>PTPN11</i> mutations in childhood acute myeloid leukaemia 由 Marco Tartaglia, Simone Martinelli, Ivano Iavarone, Giovanni Cazzaniga, Mônica Glória Neumann Spínelli, Emanuela Giarin, Valentina Petrangeli, Claudio Carta, Riccardo Masetti, Maurizio Aricò, Franco Locatelli, Giuseppe Basso, M Sorcini, Andrea Pession, Andrea Biondi
出版 2005Artigo -
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Diversity and Functional Consequences of Germline and Somatic PTPN11 Mutations in Human Disease 由 Marco Tartaglia, Simone Martinelli, Lorenzo Stella, Gianfranco Bocchinfuso, Elisabetta Flex, Viviana Cordeddu, Giuseppe Zampino, Ineke van der Burgt, Antonio Palleschi, Tamara C. Petrucci, M Sorcini, Claudia Schoch, Robin Foà, Peter D. Emanuel, Bruce D. Gelb
出版 2006Artigo -
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Risk factors for congenital hypothyroidism: results of a population case-control study (1997–2003) 由 Emanuela Medda, Antonella Olivieri, Maria Antonietta Stazi, M. E. Grandolfo, Cristina Fazzini, Mariangiola Baserga, M Burroni, E Cacciari, Francesca Calaciura, Alessandra Cassio, Luca Chiovato, Pietro Costa, Daniela Leonardi, Maria Martucci, L Moschini, Severo Pagliardini, Giuseppe Parlato, A Pignero, Aldo Pinchera, Danielle Sala, Lidia Sava, Vera Stoppioni, Francesco Tancredi, Fabiola Valentini, Riccardo Vigneri, M Sorcini
出版 2005Artigo
相关主题
Biology
Genetics
Internal medicine
Medicine
Gene
Congenital hypothyroidism
KRAS
Mutation
PTPN11
Pediatrics
Thyroid
Cancer research
Environmental health
Etiology
Germline
Germline mutation
Immunology
Noonan syndrome
Obstetrics
Population
Pregnancy
Biochemistry
Cancer
Case-control study
Cell biology
Cell surface receptor
Chemistry
Colorectal cancer
Confidence interval
Congenital malformations