Lv75
3420 积分 2021-01-07 加入
Genotype–phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome
3小时前
已完结
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system
3小时前
已完结
Prenatal detection of 5q14.3 duplication including MEF2C and brain phenotype
29天前
已完结
MEF2C deletions and mutations versus duplications: A clinical comparison
29天前
已完结
Peutz-Jeghers syndrome is caused by mutations in a novel serine threoninekinase
1个月前
已完结
Geographic tongue: What is this disease
4个月前
已完结
TMEM231Gene Conversion Associated with Joubert and Meckel-Gruber Syndromes in the Same Family
1年前
已完结
Genetic Screening in Patients with Ovarian Dysfunction
1年前
已完结
Pancreatic cancer risk variant in LINC00673 creates a miR-1231 binding site and interferes with PTPN11 degradation
2年前
已完结
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