Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation-Reference-Cited by-同舟云学术

Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation

Published:2020-09-01 Issue:9 Volume:24 Page:600-607
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Bilal Muhammad¹,Hayat Amir²,Umair Muhammad³,Ullah Asmat¹⁴⁵,Khawaja Sundus⁶,Malik Erum⁷,Burmeister Margit⁵,Bibi Nousheen⁸,Umm-e-Kalsoom ⁹,Memon Muhammad Iqbal¹⁰,Basit Sulman¹¹,Ahmad Wasim¹,Khan Bushra²

Affiliation:

1. Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.

2. Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan.

3. Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.

4. Department of Molecular Biology, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, Pakistan.

5. Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.

6. Department of Biotechnology, University of Azad Jammu & Kashmir, Muzaffarabad, Pakistan.

7. Department of Biochemistry, Shah Abdul Latif University, Khairpur, Pakistan.

8. Department of Bioinformatics, Shaheed Benazir Bhutto Women University, Peshawar, Pakistan.

9. Department of Biochemistry, Hazara University Mansehra, Mansehra, Pakistan.

10. Department of Anesthesia and Critical Care, PIMS, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, Pakistan.

11. Center for Genetics and Inherited Diseases, Taibah University, Medina, Saudi Arabia.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2020.0024

Reference31 articles.

1. Wnt gene expression in the post-natal growth plate: Regulation with chondrocyte differentiation

2. Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families

3. Regulation of osteoblastogenesis and bone mass by Wnt10b

Cited by 4 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. A complex structural variant near SOX3 causes X-linked split-hand/foot malformation;Human Genetics and Genomics Advances;2023-07

2. The role of WNT10B in physiology and disease: A 10-year update;Frontiers in Cell and Developmental Biology;2023-02-06

3. Sequence Variants in the <i>WNT10B</i> Underlying Non-Syndromic Split-Hand/Foot Malformation;Molecular Syndromology;2023

4. Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation;BMC Medical Genomics;2022-07-13