المؤلفون: Janhawi Kelkar, Miriam DiMaio, Deqiong Ma, Hui Zhang

المصدر: Global Medical Genetics, Vol 11, Iss 01, Pp 100-112 (2024)

مصطلحات موضوعية: chromosome 2 uniparental disomy, sepiapterin reductase deficiency, genomic imprinting, Genetics, QH426-470, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2699-9404

URL الوصول: https://doaj.org/article/4eb643cea5714bf28179c8a5c6d6c2be

المؤلفون: Kelkar J; Division of Medical Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, New York, United States., DiMaio M; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, United States., Ma D; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, United States., Zhang H; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, United States.

المصدر: Global medical genetics [Glob Med Genet] 2024 Mar 26; Vol. 11 (1), pp. 100-112. Date of Electronic Publication: 2024 Mar 26 (Print Publication: 2024).

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Thieme Country of Publication: Germany NLM ID: 101769583 Publication Model: eCollection Cited Medium: Internet ISSN: 2699-9404 (Electronic) Linking ISSN: 26999404 NLM ISO Abbreviation: Glob Med Genet Subsets: PubMed not MEDLINE