[<b>Clinical features and genetic mutation analysis of the hereditary dentin dysplasia type</b> Ⅰ <b>family</b>]. [PDF]
Deng Z +7 more
europepmc +1 more source
[<i>CNKSR2</i> gene variants causing Houge type of X-linked syndromic intellectual developmental disorder: Seven cases and literature review]. [PDF]
Duan H, Xiong J, Pang N, Yin F, Peng J.
europepmc +1 more source
[Effectiveness of T <sub>1</sub> nerve root transection in treatment of spastic hand contracture in cerebral palsy]. [PDF]
Xu Y +7 more
europepmc +1 more source
[Clinical Challenges in the Diagnosis and Management of Fetal Esophageal Atresia: From Prenatal Diagnosis and Surgical Intervention to Prognostic Management]. [PDF]
Sun M, Zhou F, Wang X, Wan L, Yu H.
europepmc +1 more source
[Lapidus arthrodesis combined with middle metatarsal base rotation osteotomy in treatment of hallux valgus with metatarsus adductus]. [PDF]
Shang L +7 more
europepmc +1 more source
[Factors influencing pregnancy decision-making among parents of fetuses with congenital heart disease]. [PDF]
Mao X +5 more
europepmc +1 more source
[Comparison of effectiveness of multiple metatarsal osteotomy and first metatarsophalangeal arthrodesis for severe metatarsal adductus hallux valgus deformity]. [PDF]
Lan S, Li X, Xu X, Zhu Y.
europepmc +1 more source
[Discussion on the application of clear aligner treatment in multidisciplinary complex cases]. [PDF]
Lai W.
europepmc +1 more source
[Analysis of familial intrahepatic cholestasis caused by ubiquitin-specific peptidase 53 gene mutation]. [PDF]
Wang H, Zheng X, Yu MM, Yu ZD, Wang YS.
europepmc +1 more source

