Mowat-Wilson syndrome detected by using high resolution microarray

Gene

Volumn 532, Issue 2, 2013, Pages 307-309

  Park, Jae Young ^a   Cho, Eun Hae ^b   Lee, Eun Hee ^b   Kang, You Sun ^b   Jun, Kyung Ran ^a   Hur, Yun Jung ^a  

^a Inje University College of Medicine   (South Korea)

^b Green Cross Company   (South Korea)

Author keywords

Microarray; Mowat Wilson syndrome; ZEB2

Indexed keywords

ARTICLE; ASTIGMATISM; BAYLEY SCALES OF INFANT DEVELOPMENT; BRAIN DISEASE; CASE REPORT; CHROMOSOME ANALYSIS; COGNITIVE DEFECT; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CONSTIPATION; CONVERGENT STRABISMUS; CORPUS CALLOSUM; CORPUS CALLOSUM AGENESIS; DEPRESSION; ECHOCARDIOGRAPHY; EXTERNAL EAR MALFORMATION; FACE DYSMORPHIA; FACIES; FAILURE TO THRIVE; FEMALE; FEVER; GENE; GENE DELETION; GENETIC ASSOCIATION; GTDC1 GENE; HEART ATRIUM SEPTUM DEFECT; HIGH RESOLUTION MICROARRAY ANALYSIS; HIRSCHSPRUNG DISEASE; HUMAN; HUMAN GENOME; HYDRONEPHROSIS; HYPERTELORISM; INFANT; INFANTILE SPASM; KARYOTYPE; KARYOTYPING; LANGUAGE DELAY; LIP MALFORMATION; MENTAL DEFICIENCY; MICROARRAY ANALYSIS; MICROCEPHALY; MICROGNATHIA; MOWAT WILSON SYNDROME; MUSCLE HYPOTONIA; MUSCLE TONE; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOLOGY; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; PSYCHOMOTOR RETARDATION; SPASTICITY; TENDON REFLEX; URINARY TRACT MALFORMATION; ZEB2 GENE;

GLYCOSYLTRANSFERASE-LIKE DOMAIN CONTAINING 1; GTDC1; MICROARRAY; MOWAT-WILSON SYNDROME; MWS; ZEB2; ZINC FINGER E-BOX PROTEIN 2;

ABNORMALITIES, MULTIPLE; COMPARATIVE GENOMIC HYBRIDIZATION; FACE; FACIES; FEMALE; HIRSCHSPRUNG DISEASE; HUMANS; INFANT; INTELLECTUAL DISABILITY; MICROCEPHALY; MOLECULAR DIAGNOSTIC TECHNIQUES; PSYCHOMOTOR DISORDERS;

EID: 84886747808     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2013.07.067     Document Type: Article

References (6)

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