Next-Generation sequencing and molecular diagnosis in musculoskeletal disorders-Reference-Cited by-同舟云学术

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Next-Generation sequencing and molecular diagnosis in musculoskeletal disorders

Published:2017 Issue:2 Volume:1 Page:23
ISSN:2589-1219
Container-title:Journal of Musculoskeletal Surgery and Research
language:en
Short-container-title:J Musculoskelet Surg Res

Author:

Basit Sulman

Publisher

Scientific Scholar

Reference16 articles.

1. Basit S, Alharby E, Albalawi AM, Khoshhal KI. Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2. Congenit Anom (Kyoto) 2017. doi: 10.1111/cga.12235.

Cited by 2 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. Association Between TPM1 Gene Polymorphisms and Idiopathic Congenital Talipes Equinovarus Risk in a Chinese Population;Genetic Testing and Molecular Biomarkers;2021-05-01

2. Further Evidence of a Recessive Variant in COL1A1 as an Underlying Cause of Ehlers–Danlos Syndrome: A Report of a Saudi Founder Mutation;Global Medical Genetics;2020-12

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