Williams-Beuren Syndrome With Primary Hyperparathyroidism: A Rare Diagnosis In A Rare Genetic Syndrome
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Elsevier BV
Reference16 articles.
1. Williams-Beuren Syndrome;Pober;N Engl J Med,2010
2. Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome;Sforzini;Pediatr Nephrol,2002
3. Molecular and clinical correlation study of Williams-Beuren syndrome: no evidence of molecular factors in the deletion region or imprinting affecting clinical outcome;Wang;Am J Med Genet,1999
4. Prevalence estimation of Williams syndrome;Strømme;J Child Neurol,2002
5. Severe type of infantile hypercalcemia;Schlesinger;Br Med J,1956
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Incidental Diagnosis of Williams Syndrome in an Adult With Recurrent Hypercalcemia;JCEM Case Reports;2023-12-15
2. Assessment of Multiplex Ligation-Dependent Probe Amplification (MLPA) as a diagnostic test for Egyptian patients with Williams-Beuren syndrome;Gene Reports;2020-09
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