Jihong Hao

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Topics

Allogeneic Hematopoietic Stem Cell Transplantation

Transcription Factor

Bioinformatics Analysis

Top Venues

Orphanet journal of rare diseases

Clinical chemistry and laboratory medicine

International journal of laboratory hematology

This page only lists publications with an associated author ORCID identifier.

Publications

Ziyi An, Xuening Hou, Yiping Yang, Jie Gao, Jihong Hao
First reported co-occurrence of Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia with pseudo Chediak-Higashi anomaly and complex karyotype. Clinical chemistry and laboratory medicine 62 (9) (2024)
Ziyi An, Xuening Hou, Yiping Yang, Jie Gao, Jihong Hao
First reported co-occurrence of Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia with pseudo Chediak-Higashi anomaly and complex karyotype. Clinical chemistry and laboratory medicine (2024)
Ziyi An, Xuening Hou, Yiping Yang, Jie Gao, Jihong Hao
First reported co-occurrence of Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia with pseudo Chediak-Higashi anomaly and complex karyotype. Clinical chemistry and laboratory medicine 62 (9) (2024)
Xin Ji, Xuening Hou, Xin Guo, Yifeng Sun, Futian Ma, Jihong Hao
Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome. Orphanet journal of rare diseases 17 (1) (2022)
Xin Ji, Xuening Hou, Xin Guo, Yifeng Sun, Futian Ma, Jihong Hao
Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome. Orphanet journal of rare diseases 17 (1) (2022)
Xin Ji, Xuening Hou, Xin Guo, Yifeng Sun, Futian Ma, Jihong Hao
Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome. Orphanet journal of rare diseases 17 (1) (2022)
Xin Ji, Xuening Hou, Xin Guo, Yifeng Sun, Futian Ma, Jihong Hao
Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome. Orphanet journal of rare diseases 17 (1) (2022)
Xin Ji, Xuening Hou, Xin Guo, Yifeng Sun, Futian Ma, Jihong Hao
Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome. Orphanet journal of rare diseases 17 (1) (2022)
Yi Xu, Chen Liu, Zhi Zhang, Yueyang Tian, Jihong Hao
The role of Periodic Acid Schiff stain on bone marrow smear to rapid identification of Talaromyces marneffei in a HIV-positive patient. International journal of laboratory hematology 43 (3) (2020)
Xiaoqiang Lian, Chen Liu, Xuening Hou, Wenchao Zhang, Jihong Hao
Evans syndrome in a female with erythrophagocytosis by monocytes in peripheral blood smear. International journal of laboratory hematology 42 (4) (2020)
Xin Guo, Xiaoqiang Lian, Wenchao Zhang, Jihong Hao
A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree. Clinical chemistry and laboratory medicine 56 (7) (2019)