Literature DB >> 30985307

Phenotypic delineation of a 12q21 deletion syndrome.

Caoimhe S McKenna1, Nivedita Saxena2, Tabib A Dabir1, June Jones1, Geoff Smith1, Patrick J Morrison1,3.   

Abstract

Year:  2019        PMID： 30985307     DOI： 10.1097/MCD.0000000000000274

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  2 in total

Review 1.  12q21 Interstitial Deletions: Seven New Syndromic Cases Detected by Array-CGH and Review of the Literature.

Authors:  Maria Paola Recalcati; Ilaria Catusi; Maria Garzo; Serena Redaelli; Marta Massimello; Silvia Beatrice Maitz; Mattia Gentile; Emanuela Ponzi; Paola Orsini; Anna Zilio; Annamaria Montaldi; Annapaola Calò; Anna Paola Capra; Silvana Briuglia; Maria Angela La Rosa; Lucia Grillo; Corrado Romano; Sebastiano Bianca; Michela Malacarne; Martina Busè; Maria Piccione; Lidia Larizza
Journal:  Genes (Basel)       Date:  2022-04-27       Impact factor: 4.141

2.  A New 12q21 Deletion Syndrome: A Case Report and Literature Review.

Authors:  Alessandra Di Nora; Greta De Costa; Alessia Di Mari; Marco Montemagno; Vito Pavone; Piero Pavone
Journal:  Glob Med Genet       Date:  2022-07-21
  2 in total

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