Yunlan Xu

发表

A Novel Nonsense GLI3 Variant Is Associated With Polydactyly and Syndactyly in a Family by Blocking the Sonic Hedgehog Signaling Pathway

Zhiyan Zhan, Yanxin Li, Hong Jiang, 2020, Frontiers in Genetics.

Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly

Bo Wang, Yun-lan Xu, Ying Xiang, 2017, Developmental dynamics : an official publication of the American Association of Anatomists.

Exome sequencing reveals a novel nonsense mutation of GLI3 in a Chinese family with ‘non-syndromic’ pre-axial polydactyly

Qi-hua Fu, Zhigang Wang, Yun-lan Xu, 2016, Journal of Human Genetics.

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

Yiping Shen, J. Gusella, V. Rosen, 2016, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly

Bo Wang, Guoling You, Zhigang Wang, 2017, International journal of molecular sciences.

Clinical study of 459 polydactyly cases in China, 2010 to 2014

Zhigang Wang, Yun-lan Xu, Ying Xiang, 2016, Congenital anomalies.

Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing

Bo Wang, Guoling You, Zhigang Wang, 2021, Computational and structural biotechnology journal.

Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients.

Yiping Shen, Jian Wang, Yuchan Li, 2014, Clinica chimica acta; international journal of clinical chemistry.

Risk factors for refracture of the forearm in children treated with elastic stable intramedullary nailing

Yuchan Li, Zhigang Wang, Bingqiang Han, 2018, International Orthopaedics.

Exome sequencing reveals a novel PTHLH mutation in a Chinese pedigree with brachydactyly type E and short stature.

Yiping Shen, Y. An, Jian Wang, 2015, Clinica chimica acta; international journal of clinical chemistry.

Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly

Jian Wang, Bo Wang, Niu Li, 2017, Congenital anomalies.

Pathophysiology of Hip Disorders in Patients with Mucopolysaccharidosis IVA

S. Tomatsu, Zhigang Wang, Kaiying Shen, 2020, Diagnostics.

Titanium elastic nailing versus locking compression plating in school-aged pediatric subtrochanteric femur fractures

Kaiying Shen, Yun-lan Xu, Jingxia Bian, 2018, Medicine.