Mowat-Wilson syndrome: The first two Malaysian cases

Singapore Medical Journal

Volumn 51, Issue 3, 2010, Pages

  Balasubramaniam, S ^a   Keng, W T ^a   Ngu, L H ^a   Michel, L G ^b   Irina, G ^a  

^a HOSPITAL KUALA LUMPUR   (Malaysia)

^b HENRI MONDOR HOSPITAL   (France)

Author keywords

Congenital anomaly syndrome; Hirschsprung disease; Mental retardation; Mowat wilson syndrome; Zeb2 gene

Indexed keywords

CARBAMAZEPINE; CLONAZEPAM; HOMEODOMAIN PROTEIN; UNCLASSIFIED DRUG; ZINC FINGER E BOX BINDING HOMEOBOX 2 PROTEIN;

ANAMNESIS; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COLOSTOMY; CONSTIPATION; DEVELOPMENTAL DISORDER; ECHOCARDIOGRAPHY; FEMALE; GENE MUTATION; GENETIC DISORDER; HEART ATRIUM SEPTUM DEFECT; HEART MURMUR; HIRSCHSPRUNG DISEASE; HUMAN; MALAYSIA; MENTAL DEFICIENCY; MOWAT WILSON SYNDROME; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PATENT DUCTUS ARTERIOSUS; POLYMERASE CHAIN REACTION; SEIZURE;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; CONSTIPATION; EPILEPSY; FEMALE; GENE DELETION; HIRSCHSPRUNG DISEASE; HOMEODOMAIN PROTEINS; HUMANS; MALAYSIA; REPRESSOR PROTEINS;

EID: 77951916275     PISSN: 00375675     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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