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Ding, Hongke
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1

Two fetuses of hereditary tubulinopathies with TUBB deficie..:

Zeng, Yimo ; Ding, Hongke ; Qi, Yiming...
QJM: An International Journal of Medicine.  , 2024
Link: https://doi.org/10.1093/..
 
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2

High positive predictive value of CNVs detected by clinical..:

Zeng, Yimo ; Ding, Hongke ; Wang, Xingwang...
Journal of Translational Medicine.  22 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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3

Characterization of a wheat stable QTL for spike length and..:

Ding, Hongke ; Wang, Chenyang ; Cai, Yibiao...
BMC Plant Biology.  24 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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4

A novel 1p13.2 deletion associates with neurodevelopmental ..:

Yu, Lihua ; Ding, Hongke ; Liu, Min...
BMC Medical Genomics.  16 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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5

Exome sequencing in fetuses with short long bones detected ..:

Huang, Yanlin ; Liu, Chang ; Ding, Hongke...
Frontiers in Genetics.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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6

A spectrum of clinical severity of recessive titinopathies ..:

Qi, Yiming ; Ji, Xueqi ; Ding, Hongke...
Frontiers in Genetics.  13 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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7

When NIPT meets WES, prenatal diagnosticians face the dilem..:

Ji, Xueqi ; Li, Qiongmei ; Qi, Yiming...
Frontiers in Genetics.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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8

Clinical utility of chromosomal microarray analysis and who..:

Shi, Xiaomei ; Ding, Hongke ; Li, Chen...
Annals of Medicine.  55 (2023)  1 - p. , 2023
Link: https://doi.org/10.1080/..
 
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9

A novel non-sense variant in the OFD1 gene caused Joubert s..:

Li, Chen ; Wang, Xingwang ; Li, Fake...
Frontiers in Genetics.  13 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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10

Next-generation sequencing facilitates genetic diagnosis an..:

Liu, Chang ; Huang, Yanlin ; Zhang, Yan...
International Journal of Pediatric Otorhinolaryngology.  161 (2022)  - p. 111258 , 2022
Link: https://doi.org/10.1016/..
 
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11

Paternal De Novo Variant of TAOK1 in a Fetus With Structura..:

Yu, Lihua ; Yang, Chaoxiang ; Shang, Ning...
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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12

Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogres..:

Qi, Yiming ; Ji, Xueqi ; Ding, Hongke...
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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13

A Retrospective Cohort Analysis of the Genetic Assay Result..:

Liu, Qian ; Wei, Ran ; Lu, Jian...
International Journal of General Medicine.  15 (2022)  - p. 5775-5784 , 2022
Link: https://doi.org/10.2147/..
 
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14

Phelan–McDermid Syndrome in Pediatric Patients With Novel M..:

Chen, Liang ; Yao, Zhi-ye ; Wu, Xiangtao...
Frontiers in Pediatrics.  10 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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15

A Novel Multi-Exon Deletion of PACS1 in a Three-Generation ..:

Liu, Yuan ; Ding, Hongke ; Yan, Tizhen...
Frontiers in Genetics.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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