Author:
Spazzapan Peter,Arnaud Eric,Baujat Genevieve,Nizon Mathilde,Malan Valerie,Brunelle Francis,Di Rocco Federico
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Reference26 articles.
1. Lajeunie E, Le Merrer M, Marchac D, Renier D (1998) Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patients. Am J Med Genet 75(2):211–215
2. Kini U, Hurst JA, Byren JC, Wall SA, Johnson D, Wilkie AO (2010) Etiological heterogeneity and clinical characteristics of metopic synostosis: Evidence from a tertiary craniofacial unit. Am J Med Genet A 152A(6):1383–1389
3. Abreu LS, Brassesco MS, Moreira ML, Pina-Neto JM (2014) Case report. Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome. Genet Mol Res 13(2):4302–4310
4. Christ LA, Crowe CA, Micale MA, Conroy JM, Schwartz S (1999) Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome. Am J Hum Genet 65(5):1387–1395
5. Faas BH, de Leeuw N, Mieloo H, Bruinenberg J, de Vries BB (2007) Further refinement of the candidate region for monosomy 9p syndrome. Am J Med Genet 143A(19):2353–2356
Cited by
21 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献