Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report

BACKGROUND: Except for terminal deletions that lead to Jacobsen syndrome, interstitial deletions involving the long arm of chromosome 11 are not frequently reported. A clinically distinct phenotype is usually observed in these cases, and no clear genotype-phenotype correlation is proposed. RESULTS:...

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Detalles Bibliográficos
Autores principales: Krgovic, Danijela, Marcun Varda, Natasa, Zagorac, Andreja, Kokalj-Vokac, Nadja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170628/
https://www.ncbi.nlm.nih.gov/pubmed/21859473
http://dx.doi.org/10.1186/1755-8166-4-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170628/
https://www.ncbi.nlm.nih.gov/pubmed/21859473
http://dx.doi.org/10.1186/1755-8166-4-17

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