Genetic architecture of retinoic-acid signaling-associated ocular developmental defects
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-019-02052-2.pdf
Reference171 articles.
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3. Alabdullatif MA, Al Dhaibani MA, Khassawneh MY, El-Hattab AW (2017) Chromosomal microarray in a highly consanguineous population: diagnostic yield, utility of regions of homozygosity, and novel mutations. Clin Genet 91:616–622
4. Abu-Abed S, MacLean G, Fraulob V et al (2002) Differential expression of the retinoic acid-metabolizing enzymes CYP26A1 and CYP26B1 during murine organogenesis. Mech Dev 110:173–177
5. Aldahmesh MA, Khan AO, Hijazi H, Alkuraya FS (2013) Mutations in ALDH1A3 cause microphthalmia: Mutations in ALDH1A3 cause microphthalmia. Clinical Genetics 84:128–131. https://doi.org/10.1111/cge.12184
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