المؤلفون: Tang Lan-Fang, Qin Lu, LV Jian-Hai, Zhang Fei-Zhou

المصدر: Journal of clinical research in pediatric endocrinology. 14(3)

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Growth retardation, business.industry, Endocrinology, Diabetes and Metabolism, Point mutation, Chromosome, Midface hypoplasia, Kidney dysplasia, Endocrinology, Pediatrics, Perinatology and Child Health, Genotype, medicine, AMMECR1 gene, In patient, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7aebe373424e7f5bbff6da8c20d4ee0
https://pubmed.ncbi.nlm.nih.gov/33535730

المؤلفون: Qin L; Children’s Hospital of Zhejiang University School of Medicine, Department of Pulmonology, Zhejiang, China, Zhang FZ; Children’s Hospital of Zhejiang University School of Medicine, Department of Pulmonology, Zhejiang, China, Lv JH; Shangyu People’s Hospital, Clinic of Pediatrics, Zhejiang, China, Tang LF; Shangyu People’s Hospital, Clinic of Pediatrics, Zhejiang, China

المصدر: Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2022 Aug 25; Vol. 14 (3), pp. 339-343. Date of Electronic Publication: 2021 Feb 04.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Galenos Yayınevi Country of Publication: Turkey NLM ID: 101519456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1308-5735 (Electronic) NLM ISO Abbreviation: J Clin Res Pediatr Endocrinol Subsets: PubMed not MEDLINE; MEDLINE