Lv3
340 积分 2023-03-01 加入
(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B
1个月前
已完结
Genotype phenotype correlations in pseudohypoparathyroidism type 1a patients: a systemic review
1个月前
已完结
Pseudohypoparathyroidism andGNASEpigenetic Defects: Clinical Evaluation of Albright Hereditary Osteodystrophy and Molecular Analysis in 40 Patients
1个月前
已完结
Familial gastrointestinal stromal tumor with hyperpigmentation: Association with a germline mutation of the c-kit gene
1个月前
已完结
Multiple lentigines and cutaneous hyperpigmentation caused by a KIT mutation
1个月前
已完结
[Anti-disturbance Fetal Heart Rate System Based on Combined Maternal-fetal Monitoring]
4个月前
已关闭
ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
4个月前
已完结
Epidermolysis bullosa
4个月前
已完结
Ultrastructure and molecular pathogenesis of epidermolysis bullosa
7个月前
已完结
Introduction and Methodology: Standards of Care in Diabetes—2024
8个月前
已完结
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