Paternal germline mosaicism for a GPC3 deletion in X-linked Simpson-Golabi-Behmel syndrome

Author:

Agatep Ron12,Shuman Cheryl34,Steele Leslie54,Parkinson Nicole54,Weksberg Rosanna3467,Stockley Tracy L.89

Affiliation:

1. Department of Medical Genetics; McGill University Health Centre; Montreal QC Canada

2. Department of Human Genetics; McGill University; Montreal QC Canada

3. Division of Clinical and Metabolic Genetics; The Hospital for Sick Children; Toronto Ontario Canada

4. Department of Molecular Genetics; University of Toronto; Toronto Ontario Canada

5. Department of Paediatric Laboratory Medicine; The Hospital for Sick Children; Toronto Ontario Canada

6. Program in Genetics & Genome Biology; Research Institute, The Hospital for Sick Children; Toronto Ontario Canada

7. Institute of Medical Science; University of Toronto; Toronto Ontario Canada

8. Department of Laboratory Medicine and Pathobiology; The University of Toronto; Toronto Ontario Canada

9. Molecular Diagnostics; University Health Network

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference10 articles.

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. Simpson–Golabi–Behmel syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2024-05-20

2. CUGC for Simpson-Golabi-Behmel syndrome (SGBS);European Journal of Human Genetics;2019-01-25

3. Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature;Human Mutation;2018-04-24

4. Zebrafish Developmental Models of Skeletal Diseases;Current Topics in Developmental Biology;2017

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