Deletion of chr7p22 and chr15q11: Two Familial Cases of Immune Deficiency: Extending the Phenotype Toward Dysimmunity

Background: We report here two new familial cases of associated del15q11 and del7p22, with the latter underlining the clinical variability of this deletion. Two siblings patients presented a similar familial imbalanced translocation, originating from a balanced maternal translocation, with deletions...

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Detalles Bibliográficos
Autores principales: Sloboda, Natacha, Sorlin, Arthur, Valduga, Mylène, Beri-Dexheimer, Mylène, Bilbault, Claire, Fouyssac, Fanny, Becker, Aurélie, Lambert, Laëtitia, Bonnet, Céline, Leheup, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707040/
https://www.ncbi.nlm.nih.gov/pubmed/31474980
http://dx.doi.org/10.3389/fimmu.2019.01871

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707040/
https://www.ncbi.nlm.nih.gov/pubmed/31474980
http://dx.doi.org/10.3389/fimmu.2019.01871

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