Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome

Clinical Genetics

Volumn 82, Issue 3, 2012, Pages 240-247

  Sheikhzadeh, S ^a   Kade, C ^a   Keyser, B ^b   Stuhrmann, M ^b   Arslan Kirchner, M ^b   Rybczynski, M ^a   Bernhardt, A M ^a   Habermann, C R ^a   Hillebrand, M ^a   Mir, T ^a   Robinson, P N ^c   Berger, J ^a   Detter, C ^a   Blankenberg, S ^a   Schmidtke, J ^b   von Kodolitsch, Y ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b HANNOVER MEDICAL SCHOOL   (Germany)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

FBN1; Genotype; Marfan syndrome; Phenotype; TGFBR2

Indexed keywords

FIBRILLIN 1; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 2;

ADOLESCENT; ADULT; AGED; ARTICLE; BIOMETRY; CONTROLLED STUDY; DISEASE CLASSIFICATION; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MARFAN SYNDROME; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; FEMALE; GENOTYPE; HUMANS; MALE; MARFAN SYNDROME; MIDDLE AGED; PHENOTYPE;

EID: 84865099388     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2011.01771.x     Document Type: Article

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