Detalhe da pesquisa
1.
Investigation of the mechanism of copy number variations involving the α-globin gene cluster on chromosome 16: two case reports and literature review.
Mol Genet Genomics
; 298(1): 131-141, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36326959
2.
A Rare Hb H Hydrops Fetalis Syndrome Caused by the - -SEA Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese Patient.
Hemoglobin
; 42(4): 278-280, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30486690
3.
Target capture next-generation sequencing in non-inversion haemophilia: an alternative approach.
Br J Haematol
; 189(4): e168-e170, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32190902
4.
[The value of MCV, MCH and HbA(2) in laboratory screening of thalassemia].
Zhonghua Fu Chan Ke Za Zhi
; 47(2): 96-100, 2012 Feb.
Artigo
em Zh
| MEDLINE | ID: mdl-22455739
5.
The spectrum of FVIII gene variants detected by next generation sequencing in 236 Chinese non-inversion hemophilia A pedigrees.
Thromb Res
; 202: 8-13, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33706050
6.
Correction to: Genetic and evolutionary analysis of enterovirus 71 base dinucleotide.
Virusdisease
; 31(1): 66, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32207753
7.
Genetic and evolutionary analysis of enterovirus 71 base dinucleotide.
Virusdisease
; 31(1): 61-65, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32211457
8.
Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations.
Mol Genet Genomic Med
; 8(11): e1482, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32875744
9.
Different Clinical Phenotypes Caused by Three F8 Missense Mutations in Three Chinese Families with Moderate Hemophilia A.
DNA Cell Biol
; 39(9): 1685-1690, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32589464