Clinical manifestations in 17 Greek patients with Goldenhar syndrome

Genetic Counseling

Volumn 17, Issue 3, 2006, Pages 359-370

  Touliatou, Vassiliki ^a   Fryssira, H ^a   Mavrou, A ^a   Kanavakis, E ^a   Kitsiou Tzeli, S ^a  

^a UNIVERSITY OF ATHENS   (Greece)

Author keywords

Clinical manifestations; Diagnosis; Goldenhar syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CARDIOVASCULAR MALFORMATION; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONDUCTION DEAFNESS; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; DISEASE SEVERITY; EAR DYSPLASIA; EYE MALFORMATION; FACIAL NERVE PARALYSIS; FEMALE; GASTROINTESTINAL MALFORMATION; GENETIC COUNSELING; GOLDENHAR SYNDROME; GREECE; HEARING LOSS; HUMAN; INFANT; KARYOTYPE; MALE; MANDIBLE HYPOPLASIA; MENTAL DEFICIENCY; MONOZYGOTIC TWINS; MORPHOLOGICAL TRAIT; NEUROLOGIC DISEASE; NEWBORN; PATIENT ASSESSMENT; PHENOTYPIC VARIATION; SKELETON MALFORMATION; UROGENITAL TRACT MALFORMATION; VISUAL IMPAIRMENT;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; GOLDENHAR SYNDROME; GREECE; HUMANS; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; PHENOTYPE;

EID: 33750390404     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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