Prenatal diagnosis of Coffin‐Siris syndrome: What are the fetal features?
Author:
Affiliation:
1. Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center Affiliated to Guangzhou Medical University Guangzhou Guangdong China
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6213
Reference20 articles.
1. Coffin-Siris syndrome.
2. Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
3. Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort
4. The Coffin-Siris syndrome.
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1. De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia;BMC Medical Genomics;2024-05-24
2. Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Disease;Pediatric and Developmental Pathology;2023-11-19
3. Enhancement of phenotyping for fetal investigation using next‐generation sequencing;Ultrasound in Obstetrics & Gynecology;2023-10
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