Catel-Manzke syndrome: Two new patients and a critical review of the literature

European Journal of Medical Genetics

Volumn 51, Issue 5, 2008, Pages 452-465

  Manzke, Hermann ^a   Lehmann, Katarina ^b   Klopocki, Eva ^b   Caliebe, Almuth ^c  

^a Privat   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c UNIVERSITY OF KIEL   (Germany)

Author keywords

Array CGH; Catel Manzke syndrome; Isolated Manzke dysostosis; Molecular genetic studies; Palatodigital syndrome

Indexed keywords

ARTICLE; CASE REPORT; CATEL MANZKE SYNDROME; CHILD; CHROMOSOME ABERRATION; CLINODACTYLY; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FINGER MALFORMATION; HUMAN; HYPERPHALANGY; INDEX FINGER; INFANT; KARYOTYPE; MEDICAL LITERATURE; MUTATIONAL ANALYSIS; PIERRE ROBIN SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CLEFT PALATE; FEMALE; FINGERS; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT; KARYOTYPING; MALE; MIDDLE AGED; NUCLEIC ACID HYBRIDIZATION; PIERRE ROBIN SYNDROME; SEQUENCE ANALYSIS, DNA; SYNDROME;

EID: 50549090889     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2008.03.005     Document Type: Article

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