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1.
[Phenotypic and genetic characteristics of a child with 7p15 deletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(8): 855-858, 2020 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32761594
2.
[Gene variant analysis of a child presented with neonatal diabetes and multiple organ malformations].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(12): 1371-1375, 2020 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33306825
3.
A case report of anti-GAD65 antibody-positive autoimmune encephalitis in children associated with autoimmune polyendocrine syndrome type-II and literature review.
Front Immunol
; 14: 1274672, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38077387
4.
MAGI2-AS3 restrains proliferation, glycolysis, and triggers apoptosis in acute lymphoblastic leukemia via regulating miR-452-5p/FOXN3 pathway.
Iran J Basic Med Sci
; 25(1): 46-52, 2022 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-35656441
5.
Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type.
Front Genet
; 13: 823861, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35368703
6.
Oncogenic Long Noncoding RNA DARS-AS1 in Childhood Acute Myeloid Leukemia by Binding to microRNA-425.
Technol Cancer Res Treat
; 19: 1533033820965580, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33073700
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