Clinical refinement of the SETD5‐associated phenotype in a child displaying novel features and KBG syndrome‐like appearance

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 188; no. 5; pp. 1623 - 1625
Main Authors Pascolini, Giulia, Gnazzo, Maria, Novelli, Antonio, Grammatico, Paola
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.05.2022
Wiley Subscription Services, Inc
Subjects
Abnormalities, Multiple - genetics
Bone Diseases, Developmental - genetics
Facies
Humans
Intellectual Disability - diagnosis
Intellectual Disability - genetics
Methyltransferases - genetics
Phenotype
Phenotypes
Tooth Abnormalities - genetics
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.62679