Author/Creator: Stallone, Raffaella - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Stallone, Raffaella

1. Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome. Issue 2 (28th November 2017)

Authors:: Palumbo, Pietro; Accadia, Maria; Leone, Maria P.; Palladino, Teresa; Stallone, Raffaella; Carella, Massimo; Palumbo, Orazio
Journal:: American journal of medical genetics
Issue:: Volume 176:Issue 2(2018)
Page Start:: 391
Record Type:: Journal Article
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2. Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay. (21st May 2015)

Authors:: Palumbo, Pietro; Palumbo, Orazio; Leone, Maria Pia; Stallone, Raffaella; Palladino, Teresa; Zelante, Leopoldo; Carella, Massimo
Journal:: American journal of medical genetics
Issue:: Volume 167:Number 9(2015:Sep.)
Page Start:: 2219
Record Type:: Journal Article
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3. Microdeletion of 12q24.31: Report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms. (26th November 2014)

Authors:: Palumbo, Orazio; Palumbo, Pietro; Delvecchio, Maurizio; Palladino, Teresa; Stallone, Raffaella; Crisetti, Matteo; Zelante, Leopoldo; Carella, Massimo
Journal:: American journal of medical genetics
Issue:: Volume 167:Number 2(2015:Feb.)
Page Start:: 438
Record Type:: Journal Article
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4. Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing. (June 2017)

Authors:: Leone, Maria Pia; Palumbo, Pietro; Ortore, Rocco; Castellana, Stefano; Palumbo, Orazio; Melchionda, Salvatore; Palladino, Teresa; Stallone, Raffaella; Mazza, Tommaso; Cocchi, Roberto; Carella, Massimo
Journal:: Molecular and cellular probes
Issue:: Volume 33(2017)
Page Start:: 24
Record Type:: Journal Article
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