Novel variant in the FGD1 gene causing Aarskog-Scott syndrome.
- Published in:
- Experimental & Therapeutic Medicine, 2017, v. 13, n. 6, p. 2623, doi. 10.3892/etm.2017.4301
- By:
- Publication type:
- Article
Works by Ge, Yihua
Results: 8
1
2
Psychomotor development and attention problems caused by a splicing variant of CNKSR2.
- Published in:
- BMC Medical Genomics, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s12920-020-00844-4
- By:
- Publication type:
- Article
3
Quality of reduction and prognosis of developmental dysplasia of the hip: a retrospective study.
- Published in:
- Hip International, 2016, v. 26, n. 4, p. 355, doi. 10.5301/hipint.5000348
- By:
- Publication type:
- Article
4
A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal.
- Published in:
- Journal of Bone & Mineral Research, 2016, v. 31, n. 4, p. 882, doi. 10.1002/jbmr.2761
- By:
- Publication type:
- Article
5
Clinical study of anterior hip ultrasound (van Douveren's method)-assisted Pavlik harness.
- Published in:
- 2019
- By:
- Publication type:
- journal article
6
Complex metacarpophalangeal joint dislocation caused by inappropriate reduction procedures.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
7
The benefit of rhGH therapy in a Chinese child with 12q14 microdeletion syndrome: a case report.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2023, v. 36, n. 8, p. 798, doi. 10.1515/jpem-2023-0060
- By:
- Publication type:
- Article
8
The efficacy of gradual reduction using two-stage traction for developmental dysplasia of the hip in southern China.
- Published in:
- Frontiers in Pediatrics, 2024, p. 01, doi. 10.3389/fped.2024.1335490
- By:
- Publication type:
- Article