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1دورية أكاديمية
المؤلفون: Ottenhoff, M.J. (Myrthe), Rietman, A.B. (André), Mous, S.E. (Sabine), Plasschaert, E. (Ellen), Gawehns, D. (Daniela), Brems, H. (Hilde), Oostenbrink, R. (Rianne), Wit, M.C.Y. (Marie Claire) de, Nijs, P.F.A. (Pieter) de, Legerstee, J.S. (Jeroen), Dieleman, G.C. (Gwen), Hoopen, L.W. (Leontine) ten, Thornton, A.S. (Andrew), Nellist, M.D. (Mark), Schorry, E. (Elizabeth), Legius, E. (Eric), Moll, H.A. (Henriëtte), Elgersma, Y. (Ype)
المصدر: Genetics in Medicine
مصطلحات موضوعية: genotype–phenotype association, intelligence quotient, neurofibromatosis type 1, phenotypic variability, twin study
وصف الملف: application/pdf
العلاقة: http://repub.eur.nl/pub/124697Test; urn:hdl:1765/124697
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المؤلفون: Legius, E., Messiaen, L., Wolkenstein, P., Pancza, P., Avery, R. A., Berman, Y., Blakeley, J., Babovic-Vuksanovic, D., Cunha, K. S., Ferner, R., Fisher, M. J., Friedman, J. M., Gutmann, D. H., Kehrer-Sawatzki, H., Korf, B. R., Mautner, V. F., Peltonen, Sirkku, 1964, Rauen, K. A., Riccardi, V., Schorry, E., Stemmer-Rachamimov, A., Stevenson, D. A., Tadini, G., Ullrich, N. J., Viskochil, D., Wimmer, K., Yohay, K., Huson, S. M., Evans, D. G., Plotkin, S. R.
المصدر: Genetics in Medicine. 23:1506-1513
مصطلحات موضوعية: Medical Genetics, Medicinsk genetik, choroidal abnormalities, sequence variants, mutation analysis, gene, mosaicism, identification, reveals, Genetics & Heredity
الوصول الحر: https://gup.ub.gu.se/publication/305494Test