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Infectio, ISSN 0123-9392, 01/2016, Volume 20, Issue 1, pp. 53 - 55
El síndrome por deleción 22q11 (SD22q11) es el síndrome por deleción cromosómica más frecuente en humanos y se caracteriza por la tríada clínica que incluye... 
INFECTIOUS DISEASES
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 7/2015, Volume 35, Issue 5, pp. 501 - 511
Journal Article
Infectio, ISSN 0123-9392, Volume 20, Issue 1, pp. 53 - 55
El síndrome por deleción 22q11 (SD22q11) es el síndrome por deleción cromosómica más frecuente en humanos y se caracteriza por la tríada clínica que incluye... 
22q11 deletion syndrome | DiGeorge syndrome | Immunodeficiency | Congenital lymphopaenia | Thymic aplasia | Congenital heart disease | Thymic hypoplasia
Journal Article
Scandinavian Journal of Immunology, ISSN 0300-9475, 09/2017, Volume 86, Issue 3, pp. 171 - 178
Journal Article
Iatreia, ISSN 0121-0793, 09/2011, Volume 24, Issue 3, pp. 229 - 237
Objetivo: evaluar la utilidad de la PCR para marcadores microsatélites (PCR-STR) en la región 22q11.2 en el ADN genómico, para identificar microdeleciones en... 
MEDICINE, GENERAL & INTERNAL
Journal Article
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