Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism‐array analysis

In this paper, is reported the identification of two chimeric patients, a rare finding if sexual abnormalities are absent. However, their chimeric condition is responsible at least for the Silver–Russell phenotype observed in one of the two patients. By single nucleotide polymorphism‐array analyses,...

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Detalles Bibliográficos
Autores principales: Bottega, Roberta, Cappellani, Stefania, Fabretto, Antonella, Spinelli, Alessandro Mauro, Severini, Giovanni Maria, Aloisio, Michelangelo, Faleschini, Michela, Athanasakis, Emmanouil, Bruno, Irene, Faletra, Flavio, Pecile, Vanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418439/
https://www.ncbi.nlm.nih.gov/pubmed/30628197
http://dx.doi.org/10.1002/mgg3.546

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418439/
https://www.ncbi.nlm.nih.gov/pubmed/30628197
http://dx.doi.org/10.1002/mgg3.546

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