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1دورية أكاديمية
المؤلفون: Smith, C.E.L., Laugel-Haushalter, V., Hany, U., Best, S., Taylor, R.L., Poulter, J.A., Wortmann, S.B., Feichtinger, R.G., Mayr, J.A., Al Bahlani, S., Nikolopoulos, G., Rigby, A., Black, G.C., Watson, C.M., Mansour, S., Inglehearn, C.F., Mighell, A.J., Bloch-Zupan, A.
وصف الملف: text
العلاقة: https://eprints.whiterose.ac.uk/212916/1/jmg-2023-109728.full.pdfTest; Smith, C.E.L. orcid.org/0000-0001-8320-5105 , Laugel-Haushalter, V., Hany, U. orcid.org/0000-0002-4486-1625 et al. (15 more authors) (2024) Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of Medical Genetics. ISSN 0022-2593
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