Williams syndrome: Autosomal dominant inheritance
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference22 articles.
1. Williams syndrome.
2. HYPERCALÆMIA AND SUPRAVALVAR AORTIC STENOSIS
3. Familial Williams Syndrome
4. The Williams Syndrome
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1. Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome;Orphanet Journal of Rare Diseases;2023-09-27
2. Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders;American Journal of Medical Genetics Part A;2023-04-20
3. Identifying Genetic Etiology in Patients with Intellectual Disability: An Experience in Public Health Services in Northeastern Brazil;Journal of Pediatric Genetics;2022-11-14
4. Mid-trimester isolated bilateral rocker bottom feet leading to prenatal diagnosis of 7q11.23 microdeletion: Williams syndrome;Journal of Ultrasound;2022-01-10
5. Functional Neurological Symptom Disorder in Williams Syndrome: Case Series and Review of Relevant Literature;Journal of the Academy of Consultation-Liaison Psychiatry;2021-10
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