The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome

American Journal of Medical Genetics, Part A

Volumn 146, Issue 24, 2008, Pages 3157-3166

  Rybczynski, Meike ^a   Bernhardt, Alexander M J ^a   Rehder, Uwe ^a   Fuisting, Bettina ^a   Meiss, Ludwig ^a   Voss, Ursula ^a   Habermann, Christian ^a   Detter, Christian ^a   Robinson, Peter N ^b   Arslan Kirchner, Mine ^c   Schmidtke, Jörg ^c   Mir, Thomas S ^a   Berger, Jürgen ^a   Meinertz, Thomas ^a   Von Kodolitsch, Yskert ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

FBN1 gene; Genetic counseling; Loeys Dietz syndrome; Marfan syndrome; MASS phenotype; TGFBR1 gene; TGFBR2 gene

Indexed keywords

ADULT; AORTA ANEURYSM; AORTA DISEASE; AORTA DISSECTION; ARTICLE; BONE DISEASE; CARDIOVASCULAR RISK; CLINICAL FEATURE; CONNECTIVE TISSUE DISEASE; EYE DISEASE; FAMILY HISTORY; FEMALE; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MARFAN SYNDROME; PRIORITY JOURNAL; PROGNOSIS;

ADULT; COHORT STUDIES; FEMALE; HUMANS; MALE; MARFAN SYNDROME; MASS SCREENING; MICROFILAMENT PROTEINS; MUTATION; SYNDROME;

EID: 57149088301     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32595     Document Type: Article

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