Chromosome 1p31.1 Deletion Syndrome: Limited Expression

Chromosomal microdeletion syndromes usually present with neurological abnormalities, developmental delays, and various systemic abnormalities. 1p31 microdeletion syndrome is one of the novel microdeletion syndromes that usually presents with developmental delay, intellectual disability, various cran...

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Detalles Bibliográficos
Autores principales: Biswal, Seba, Parida, Preetinanda, Dubbudu, Aranya, Sharawat, Indar Kumar, Panda, Prateek Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061518/
https://www.ncbi.nlm.nih.gov/pubmed/33911383
http://dx.doi.org/10.4103/aian.AIAN_258_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061518/
https://www.ncbi.nlm.nih.gov/pubmed/33911383
http://dx.doi.org/10.4103/aian.AIAN_258_20

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