Goldenhar and cri-du-chat syndromes: A contiguous gene deletion syndrome?

Journal of AAPOS

Volumn 7, Issue 3, 2003, Pages 226-227

  Choong, Yee Fong ^a   Watts, Patrick ^a   Little, Elizabeth ^a   Beck, Lyn ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CAT CRY SYNDROME; CHROMOSOME 5; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 5; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; ESOPHAGUS ATRESIA; FEEDING DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC DISORDER; GOLDENHAR SYNDROME; HEARING TEST; HUMAN; INFANT; MALE; POLYTHELIA; PRIORITY JOURNAL; TACHYPNEA; TRACHEOESOPHAGEAL FISTULA;

EID: 0042026461     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1091-8531(02)42019-8     Document Type: Article

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