Two Novel Variants Associated with Brain Abnormalities in Clinical Suspicion of Arthrogryposis and Similar Phenotype in Three Children: Challenges in Offering Prenatal Diagnosis
Author:
Funder
ICMR-NIRRH
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology
Link
https://link.springer.com/content/pdf/10.1007/s13224-023-01776-6.pdf
Reference4 articles.
1. Kiefer J, Hall JG. Gene ontology analysis of arthrogryposis (multiple congenital contractures). InAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics 2019 Sep (Vol. 181, No. 3, pp. 310–326). Hoboken: Wiley
2. Stoll C, Dott B, Roth MP. Associated anomalies in cases with agenesis of the corpus callosum. Am J Med Genet A. 2019;179(10):2101–11.
3. Etchegaray A, Juarez-Peñalva S, Petracchi F, Igarzabal L. Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus. Childs Nerv Syst. 2020;36(8):1645–60.
4. Gass JM, Head BB, Shields SM, Stevenson RE, Louie RJ. Hydrocephaly associated with compound heterozygous alterations in TRAPPC12. Birth Defects Res. 2020;112(13):1028–34.
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