Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference30 articles.
1. Dhamija R, Babovic-Vuksanovic D. Hartsfield syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2018 (last updated: 3 Mar 2016).
2. Simonis N, Migeotte I, Lambert N, Perazzolo C, De Silva DC, Dimitrov B, et al. FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. J Med Genet. 2013;50:585–92.
3. Hong S, Hu P, Marino J, Hufnagel SB, Hopkin RJ, Toromanović A, et al. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome. Hum Mol Genet. 2016;25:1912–22.
4. Ornitz DM & Itoh N. The fibroblast growth factor signaling pathway. Wiley Interdisciplinary Rev Dev Biol. 2015;4:215–66.
5. Teven CM, Farina EM, Rivas J, Reid RR. Fibroblast growth factor (FGF) signaling in development and skeletal diseases. Genes Dis. 2014;1:199–213.
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