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Hong Qi

6PUBLICATIONS

6CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Foetal development and medicineReproductive medicine not elsewhere classifiedSouth-East Asian languages (excl. Indonesian)

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Publications (6)

Sort by Publication Date:

|Jun 07, 2023

Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number Variation.

Xiaohui Wen, Huanxia Xing, Keyan Qi

|Nov 02, 2022

Identification of Diagnostic Variants in <i>FGFR2</i> and <i>NPR2</i> Genes in a Chinese Family Affected by Crouzon Syndrome and Acromesomelic Dysplasia, Type Maroteaux.

JianJiang Zhu, Ran Meng, HuaWei Zhao

|Dec 05, 2021

De novo balanced reciprocal translocation mosaic t(1;3)(q42;q25) detected by prenatal genetic diagnosis: a fetus conceived using preimplantation genetic testing due to a t(12;14)(q22;q13) balanced paternal reciprocal translocation.

Shaoqin Zhang, Jianjiang Zhu, Hong Qi

|Feb 24, 2021

cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVF.

Jianjiang Zhu, Feng Hui, Xuequn Mao

|Sep 25, 2019

C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosis.

Jian Jiang Zhu, Hong Qi, Li Rong Cai

|Jul 19, 2019

Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.

Jianjiang Zhu, Hong Qi, Sha Cao

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Frequent Collaborators

5 joint publications

Jianjiang Zhu

1 joint publications

Sha Cao

1 joint publications

Yang Du

1 joint publications

Shaoqin Zhang

1 joint publications

Huanxia Xing

1 joint publications

Jing Zhang

Frequent Collaborators

5 joint publications

Jianjiang Zhu

1 joint publications

Sha Cao

1 joint publications

Yang Du

1 joint publications

Shaoqin Zhang

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