المؤلفون: Lionne N. Grootjen, Alicia F. Juriaans, Gerthe F. Kerkhof, Anita C. S. Hokken-Koelega

المصدر: Journal of Clinical Medicine; Volume 11; Issue 15; Pages: 4636

مصطلحات موضوعية: Prader-Willi syndrome, genotype–phenotype correlation, atypical deletions, SNURF-SNPRN, SNORD116

وصف الملف: application/pdf

Relation: Endocrinology & Metabolism; https://dx.doi.org/10.3390/jcm11154636

الاتاحة: https://doi.org/10.3390/jcm11154636