A Case Report of in Utero Williams Syndrome Arterial Malformation
Author:
Affiliation:
1. Department of Pathology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA
Publisher
Informa UK Limited
Subject
General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/15513815.2017.1379040
Reference5 articles.
1. Disruption of the elastin gene in adult Williams syndrome is accompanied by a paradoxical reduction in arterial stiffness
2. Severe Infantile Hypercalcemia Associated With Williams Syndrome Successfully Treated With Intravenously Administered Pamidronate
3. Organ Weights in Human Fetuses after Formalin Fixation: Standards by Gestational Age and Body Weight
4. The normal diameter of the fetal aorta and pulmonary artery: echocardiographic evaluation in utero
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1. Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome);Prenatal Diagnosis;2023-03-23
2. Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review;Frontiers in Pediatrics;2023-03-17
3. Pleiotropy of Copy Number Variation in Human Genome;Russian Journal of Genetics;2022-10
4. Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis;Molecular Cytogenetics;2022-06-28
5. Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review;Annals of Human Genetics;2019-11-11
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