SATB2 ‐associated syndrome in adolescents and adults
Author:
Affiliation:
1. Section of Genetics and Metabolism, University of Arkansas for Medical Sciences Little Rock Arkansas USA
2. Health Outcomes, College of Pharmacy, University of Rhode Island Kingston Rhode Island USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62258
Reference14 articles.
1. Clinical and molecular consequences of disease-associated de novo mutations in SATB2
2. Transition to adult health care: Setting the stage
3. Practical Steps to Help Transition Pediatric Patients to Adult Care
4. Heterozygous nonsense mutationSATB2 associated with cleft palate, osteoporosis, and cognitive defects
5. Intragenic duplication-A novel causative mechanism for SATB2-associated syndrome
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