Marfan-like habitus and familial adenomatous polyposis in two unrelated males: a significant association?

Calin, G; Wijnen, J; van der Klift, H; Ionita, A; Mulder, A; Breukel, C; Smits, R; Dauwerse, H; Hansson, K; Calin, S; Stefanescu, D; Oproiu, A; Fodde, R

Calin, G; Wijnen, J; van der Klift, H; Ionita, A; Mulder, A; Breukel, C; Smits, R; Dauwerse, H; Hansson, K; Calin, S; Stefanescu, D; Oproiu, A; Fodde, R.

Affiliation

Calin G; Gastroenterology Department, Fundeni Hospital, Bucharest, Romania.

Eur J Hum Genet ; 7(5): 609-14, 1999 Jul.

Article in En | MEDLINE | ID: mdl-10439970

Subject(s)

Adenomatous Polyposis Coli/genetics; Marfan Syndrome/genetics; Adenomatous Polyposis Coli/complications; Adult; Amino Acid Sequence; Female; Fibrillin-2; Fibrillins; Genes, APC; Humans; In Situ Hybridization, Fluorescence; Male; Marfan Syndrome/complications; Microfilament Proteins/genetics; Molecular Sequence Data; Mutation; Pedigree

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Collection: 01-internacional Database: MEDLINE Main subject: Adenomatous Polyposis Coli / Marfan Syndrome Type of study: Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Eur J Hum Genet Year: 1999 Document type: Article

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