Dental anomalies in Williams syndrome

Postgraduate Medical Journal

Volumn 76, Issue 901, 2000, Pages 712-

  Kashyap, A S ^a   Sharma, H S ^a   Kumar, P ^a  

^a ARMED FORCES MEDICAL COLLEGE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ELASTIN; PROTEIN KINASE;

AORTA SUPRAVALVULAR STENOSIS; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 7Q; CHROMOSOME DELETION; CONNECTIVE TISSUE DISEASE; DENTAL CARIES; DIET RESTRICTION; DISEASE ASSOCIATION; DISEASE COURSE; DOMINANT INHERITANCE; GENE DELETION; HUMAN; MALE; MENTAL DEFICIENCY; PHYSICAL EXAMINATION; PREOPERATIVE EVALUATION; WILLIAMS BEUREN SYNDROME;

CHILD, PRESCHOOL; DENTAL CARIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; TOOTH ABNORMALITIES; WILLIAMS SYNDROME;

EID: 0033736637     PISSN: 00325473     EISSN: None     Source Type: Journal    
DOI: 10.1136/pmj.76.901.712     Document Type: Article

References (4)

1. Williams syndrome: Autosomal dominant inheritance
2. The Williams syndrome: Evidence for possible autosomal dominant inheritance
3. Strong correlation of elastin deletions detected by FISH, with Williams syndrome: Evaluation of 235 patients
4. Deletions in the elastin gene at 7q11.23 occur in ~90% of patients with Williams syndrome