Genotype–Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review

2q37 microdeletion/deletion syndrome (2q37DS) is one of the most common subtelomeric deletion disorders, caused by a 2q37 deletion of variable size. The syndrome is characterized by a broad and diverse spectrum of clinical findings: characteristic facial dysmorphism, developmental delay/intellectual...

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Detalles Bibliográficos
Autores principales: Gavril, Eva-Cristiana, Nucă, Irina, Pânzaru, Monica-Cristina, Ivanov, Anca Viorica, Mihai, Cosmin-Teodor, Antoci, Lucian-Mihai, Ciobanu, Cristian-Gabriel, Rusu, Cristina, Popescu, Roxana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957522/
https://www.ncbi.nlm.nih.gov/pubmed/36833393
http://dx.doi.org/10.3390/genes14020465

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957522/
https://www.ncbi.nlm.nih.gov/pubmed/36833393
http://dx.doi.org/10.3390/genes14020465

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