A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype
一名被诊断患有18号染色体短臂11.1区微缺失综合征的新生儿患者表现出类似18三体综合征的表型
期刊:Case Reports in Pediatrics
影响因子:0.5
doi:10.1155/2023/2275582
Banker, Deepa; Mungala, Bhavdeep; Parekh, Zankhana; Ganatra, Shachi; Maheshwari, Vimal; Raj, Yashica; Patel, Utsav; Patel, Digant; Chamar, Kishan; Solanki, Vasu
