Genetic regulatory pathways of split‐hand/foot malformation-Reference-Cited by-同舟云学术

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Genetic regulatory pathways of split‐hand/foot malformation

Published:2018-09-10 Issue:1 Volume:95 Page:132-139
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Kantaputra Piranit N.¹²³^ORCID,Carlson Bruce M.⁴

Affiliation:

1. Center of Excellence in Medical Genetics ResearchChiang Mai University Chiang Mai Thailand

2. Division of Pediatric Dentistry, Department of Orthodontics and Pediatric DentistryFaculty of Dentistry, Chiang Mai University Chiang Mai Thailand

3. Dentaland Clinic Chiang Mai Thailand

4. Department of Anatomy and Cell BiologyUniversity of Michigan Ann Arbor Michigan

Funder

Thailand Research Fund

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13434

Reference58 articles.

1. Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation

2. Regulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defects

3. Sp6 and Sp8 Transcription Factors Control AER Formation and Dorsal-Ventral Patterning in Limb Development

4. Limb development: a paradigm of gene regulation

5. p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. People with higher systemizing traits have wider right hands;Frontiers in Psychiatry;2024-09-05

2. A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature;Cureus;2024-07-22

3. Early Prenatal Detection of Recessive Split-hand/Foot Malformation Caused by a Homozygous Variant of WNT10B;Journal of Medical Ultrasound;2024-07

4. DLX5 promotes Col10a1 expression and chondrocyte hypertrophy and is involved in osteoarthritis progression;Genes & Diseases;2023-09

5. Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes;Genes;2023-07-26

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