Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference254 articles.
1. Abdalla EM, Mostowska A, Jagodzinski PP, Dwidar K, Ismail SR (2014) A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family. Arch Oral Biol 59:722–728. doi: 10.1016/j.archoralbio.2014.04.004
2. Acevedo AC, da Fonseca JA, Grinham J, Doudney K, Gomes RR, de Paula LM, Stanier P (2010) Autosomal-dominant ankyloglossia and tooth number anomalies. J Dent Res 89:128–132. doi: 10.1177/0022034509356401
3. Acierno JS Jr, Shagoury JK, Bo-Abbas Y, Crowley WF Jr, Seminara SB (2003) A locus for autosomal recessive idiopathic hypogonadotropic hypogonadism on chromosome 19p13.3. J Clin Endocrinol Metabol 88:2947–2950. doi: 10.1210/jc.2003-030423
4. Adam MP, Hudgins L, Hannibal M (1993) Kabuki syndrome. In: Pagon RA et al. (eds) GeneReviews(R). University of Washington, Seattle University of Washington, Seattle. All rights reserved, Seattle (WA)
5. Agulnik SI et al (1996) Evolution of mouse T-box genes by tandem duplication and cluster dispersion. Genetics 144:249–254
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