Absence of maternal microchimerism in very early onset inflammatory bowel disease R1. | J Gastroenterol Hepatol;21(6): 1082-4, 2006 Jun. | MEDLINE

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Absence of maternal microchimerism in very early onset inflammatory bowel disease R1.

Boniotto, Michele; Berti, Irene; Santon, Daniela; Ventura, Alessandro; Crovella, Sergio.

J Gastroenterol Hepatol ; 21(6): 1082-4, 2006 Jun.

Article in En | MEDLINE | ID: mdl-16725006

Subject(s)

Chimerism; Genes, X-Linked/genetics; Inflammatory Bowel Diseases/genetics; Chromosomes, Human, X/genetics; Chromosomes, Human, Y/genetics; DNA Mutational Analysis; Female; Genetic Markers; Humans; In Situ Hybridization, Fluorescence; Infant; Male; Polymorphism, Genetic

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Collection: 01-internacional Database: MEDLINE Main subject: Inflammatory Bowel Diseases / Chimerism / Genes, X-Linked Limits: Female / Humans / Infant / Male Language: En Journal: J Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2006 Document type: Article

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Collection: 01-internacional Database: MEDLINE Main subject: Inflammatory Bowel Diseases / Chimerism / Genes, X-Linked Limits: Female / Humans / Infant / Male Language: En Journal: J Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2006 Document type: Article