Arama Sonuçları - Stefania Di Candia
- Gösterilen 1 - 4 sonuçlar arası kayıtlar. 4
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1
Prader-Willi Syndrome: Clinical Aspects Yazar: Elena, Grechi, Bruna, Cammarata, Benedetta, Mariani, Stefania, Di Candia, Giuseppe, Chiumello
Baskı/Yayın Bilgisi 2012Metin -
2
Persistent mild hypothyroidism associated with novel sequence variants of theDUOX2 gene in two siblings Yazar: Maria Cristina Vigone, Laura Fugazzola, I. Zamproni, Arianna Passoni, Stefania Di Candia, G Chiumello, Luca Persani, Giovanna Weber
Baskı/Yayın Bilgisi 2005Artigo -
3
Growth Hormone Therapy and Respiratory Disorders: Long-Term Follow-up in PWS Children Yazar: J. Berini, V. Spica Russotto, Paolo Castelnuovo, Stefania Di Candia, L Gargantini, Graziano Grugni, Lorenzo Iughetti, Luigi Nespoli, Luana Nosetti, G. Padoan, Alba Pilotta, Giuliana Trifirò, G Chiumello, Alessandro Salvatoni
Baskı/Yayın Bilgisi 2013Artigo -
4
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes Yazar: Silvia Russo, Luciano Calzari, Alessandro Mussa, Ester Mainini, Matteo Cassina, Stefania Di Candia, Maurizio Clementi, Sara Guzzetti, Silvia Tabano, Monica Miozzo, Silvia Maria Sirchia, Palma Finelli, Paolo Prontera, Silvia Maitz, Giovanni Sorge, Annalisa Calcagno, Mohamad Maghnie, Maria Teresa Divizia, Daniela Melis, Emanuela Manfredini, Giovanni Battista Ferrero, Vanna Pecile, Lidia Larizza
Baskı/Yayın Bilgisi 2016Artigo
Arama Araçları:
İlgili Konular
Internal medicine
Medicine
Biology
Gene
Genetics
Allele
Apnea
Beckwith–Wiedemann syndrome
Bioinformatics
Chemistry
Compound heterozygosity
Congenital hypothyroidism
DNA methylation
Endocrinology
Exon
Gene expression
Iodine
Methylation
Missense mutation
Multiplex
Multiplex ligation-dependent probe amplification
Muscle hypertrophy
Mutation
Nonsense mutation
Obstructive sleep apnea
Organic chemistry
Organification
Pediatrics
Polysomnography
Proband