Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
Periodontics,Oral Surgery,Pediatrics, Perinatology and Child Health,Orthodontics
Link
https://www.ijcpd.com/doi/pdf/10.5005/jp-journals-10005-2498
Reference19 articles.
1. 1. Simonis N, Migeotte I, Lambert N, et al. FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. J Med Genet 2013;50(9):585–592. DOI: 10.1136/jmedgenet-2013-101603
2. 2. Lansdon LA, Bernabe HV, Nidey N, et al. The use of variant maps to explore domain-specific mutations of FGFR1. J Dent Res 2017;96(11):1339–1345. DOI: 10.1177/0022034517726496
3. 3. Vilain C, Mortier G, Van Vliet G, et al. Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review. Am J Med Genet A 2019;149A(7):1476–1481. DOI: 10.1002/ajmg.a.32678
4. 4. Hartsfield JK, Bixler D, DeMeyer WE. Syndrome identification case report 119: hypertelorism associated with holoprosencephaly and ectrodactyly. Clin Dysmorphol 1984;2:27–31.
5. 5. Dhamija R, Kirmani S, Wang X, et al. Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism. Am J Med Genet A 2014;164A(9):2356–2359. DOI: 10.1002/ajmg.a.36621
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