Familial Williams Syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb00866.x/fullpdf
Reference9 articles.
1. Pathogenesis of supravalvular aortic stenosis syndrome;Antia;J. Pediat.,1967
2. Supravalvular aortic stenosis: a complex syndrome with or without mental retardation;Beuren;Birth Defects: Original Article Series,1972
3. The Williams elfin facies syndrome;Jones;Pediat.,1975
4. Supravalvular aortic stenosis. Report of a family with peculiar somatic features and normal intelligence;Lewis;Dis. Chest,1969
5. Possible dominant inheritance of the idiopathic hypercalcemic syndrome;Mehes;Hum. Hered.,1975
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2. Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review;Annals of Human Genetics;2019-11-11
3. Clinical expression of familial Williams-Beuren syndrome in a Turkish family;Journal of Pediatric Endocrinology and Metabolism;2014-01-01
4. Language, Speech and Hearing in Williams Syndrome: Intervention Approaches and Research Needs;Developmental Medicine & Child Neurology;2008-11-12
5. Elevated 1,25-dihydroxyvitamin D and normocalcaemia in presumed familial Williams syndrome;Clinical Genetics;2008-06-28
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