Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations

American Journal of Medical Genetics

Volumn 111, Issue 2, 2002, Pages 205-209

  Engels, Hartmut ^a   Bosse, Kristin ^a   Ehrbrecht, Antje ^a   Zahn, Susanne ^a   Hoischen, Alexander ^a   Propping, Peter ^a   Bindl, Lutz ^a   Reutter, Heiko ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

Cardiomegaly; Hypertrichosis; Osteochondrodysplasia

Indexed keywords

ALKALINE PHOSPHATASE;

ARTICLE; BRAIN CALCIFICATION; BRAIN SCINTISCANNING; CANTU SYNDROME; CARDIOMEGALY; CASE REPORT; CHONDRODYSPLASIA; CHROMOSOME ABERRATION; CLINICAL FEATURE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPERTRICHOSIS; LATERAL BRAIN VENTRICLE; MALE; MENTAL DEFICIENCY; NEWBORN; PRIORITY JOURNAL; PYLORUS STENOSIS; STRIATE CORTEX; TELOMERE; THALAMUS; ADULT; FEMALE; GENETICS; INFANT; KARYOTYPING; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PREGNANCY; PREGNANCY COMPLICATION; REVIEW; SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CARDIOMEGALY; CASE REPORT; CHROMOSOME ABERRATIONS; FEMALE; HUMAN; HYPERTRICHOSIS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; MENTAL RETARDATION; OSTEOCHONDRODYSPLASIAS; PREGNANCY; PREGNANCY COMPLICATIONS; SUPPORT, NON-U.S. GOV'T; SYNDROME; TELOMERE; HUMANS;

EID: 4243238318     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10560     Document Type: Article

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