3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities

BACKGROUND: Overlapping microdeletions of chromosome 3q26-3q28 have been reported in eight individuals. The common phenotype observed in these individuals include intrauterine growth restriction, short stature, microcephaly, feeding difficulties, facial dysmorphisms, limb abnormalities and developme...

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Detalles Bibliográficos
Autores principales: Barua, Subit, Pereira, Elaine M., Jobanputra, Vaidehi, Anyane-Yeboa, Kwame, Levy, Brynn, Liao, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895857/
https://www.ncbi.nlm.nih.gov/pubmed/35241116
http://dx.doi.org/10.1186/s13039-022-00587-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895857/
https://www.ncbi.nlm.nih.gov/pubmed/35241116
http://dx.doi.org/10.1186/s13039-022-00587-0

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