The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4
Author:
Funder
National Institute of Dental and Craniofacial Research
NIH Office of the Director
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00335-023-09999-8.pdf
Reference47 articles.
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3. Bourgeois P, Bolcato-Bellemin AL, Danse JM, Bloch-Zupan A, Yoshiba K, Stoetzel C, Perrin-Schmitt F (1998) The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome. Hum Mol Genet 7:945–957
4. Brewer JR, Mazot P, Soriano P (2016) Genetic insights into the mechanisms of Fgf signaling. Genes Dev 30:751–771
5. Carlton MB, Colledge WH, Evans MJ (1998) Crouzon-like craniofacial dysmorphology in the mouse is caused by an insertional mutation at the Fgf3/Fgf4 locus. Dev Dyn 212:242–249
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