Rare Diseases
Records 1 - 8 (of 8 Records) |
Query Trace: Craniosynostosis[original query]>>Reviews/Commentaries[Product Type] |
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Artificial Intelligence Applications in Diagnosing and Managing Non-syndromic Craniosynostosis: A Comprehensive Review. Amna Qamar et al. Cureus 2023 15(9) e45318 |
Apert syndrome: prenatal diagnosis challenge. Vieira Catarina et al. BMJ case reports 2019 Dec 12(12) |
Genome-wide association studies of structural birth defects: A review and commentary. Lupo Philip J et al. Birth defects research 2019 Oct |
Crouzon syndrome: Genetic and intervention review. Al-Namnam N M et al. Journal of oral biology and craniofacial research 9(1) 37-39 |
She had a lot of rashes, but dont all kids? SG Boodman, Washington Post, July 2018 |
Genetics of non-syndromic craniosynostosis. Timberlake Andrew T et al. Plastic and reconstructive surgery 2018 Mar |
Clinical genetics of craniosynostosis. Wilkie Andrew O M et al. Current opinion in pediatrics 2017 Sep |
Genetic Screening in Patients with Craniofacial Malformations. Yoon Amanda J et al. Journal of pediatric genetics 2016 Dec 5(4) 220-224 |