Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: An under-recognized association

Clinical Dysmorphology

Volumn 23, Issue 1, 2014, Pages 20-23

  Tanteles, George A ^a   Christophidou Anastasiadou, Violetta ^a  

^a CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR ZEB2; UNCLASSIFIED DRUG;

ANIRIDIA; APGAR SCORE; ARTICLE; CASE REPORT; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; FACE DISORDER; FEMALE; FRONTAL BOSSING; GENETIC DISORDER; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPERTELORISM; HYPOSPADIAS; IRIS COLOBOMA; KARYOTYPE; KARYOTYPING; MALE; MICROPHTHALMIA; MOWAT WILSON SYNDROME; MUSCLE HYPOTONIA; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PRIORITY JOURNAL; PULMONARY HYPERTENSION; RESPIRATORY DISTRESS; SEIZURE; STRABISMUS;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; FACIES; HIRSCHSPRUNG DISEASE; HUMANS; INFANT, NEWBORN; INTELLECTUAL DISABILITY; KARYOTYPE; MALE; MICROCEPHALY;

EID: 84890551994     PISSN: 09628827     EISSN: 14735717     Source Type: Journal    
DOI: 10.1097/MCD.0000000000000013     Document Type: Article

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