Detalhe da pesquisa
1.
Heterozygous CAPZA2 mutations cause global developmental delay, hypotonia with epilepsy: a case report and the literature review.
J Hum Genet
; 69(5): 197-203, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374166
2.
[Clinical characteristics of children on prolonged mechanical ventilation due to different primary diseases]. / ä¸åååç 导è´é¿ææºæ¢°éæ°æ£å¿ç临åºç¹å¾åæ.
Zhongguo Dang Dai Er Ke Za Zhi
; 26(5): 481-485, 2024 May 15.
Artigo
em Zh
| MEDLINE | ID: mdl-38802908
3.
Mutation analysis of the TUBB8 gene in primary infertile women with arrest in oocyte maturation.
Gynecol Endocrinol
; 34(10): 900-904, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29671363