Tzu-Hao Wang

发表

Association between single nucleotide polymorphisms of the estrogen receptor 1 and receptor activator of nuclear factor kappa B ligand genes and bone mineral density in postmenopausal Taiwanese.

F. Kung, Ko-en Huang, Hong-Yo Kang, 2013, Taiwanese journal of obstetrics & gynecology.

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, American journal of medical genetics. Part A.

Wnt pathway activation and ABCB1 expression account for attenuation of Proteasome inhibitor-mediated apoptosis in multidrug-resistant cancer cells

C. Tseng, Chuan‐Mu Chen, K. Choo, 2015, Cancer biology & therapy.

Abstract 3290: Glucose-regulated protein 58 modulates β-catenin protein stability in cervical adenocarcinoma

Kwang-Huei Lin, Syuan-Ling Lin, Tzu-Hao Wang, 2014 .

Rectus Sheath Hematoma During Pregnancy - A Severe but Easily Overlooked Condition: A Case Report

Yi-Hao Lin, Tzu-Hao Wang, Hsing-Tse Yu, 2004 .

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)

Chih-ping Chen, S. Chern, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2→qter)

Chih-ping Chen, C. Tzen, S. Chern, 2006, Prenatal diagnosis.

Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome

Chih-ping Chen, F. Hsieh, Y. Soong, 2008, Journal of Human Genetics.

Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1

Chih-ping Chen, C. Tzen, S. Chern, 2007, Prenatal diagnosis.

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2006, Prenatal diagnosis.

Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.

Chih-ping Chen, F. Tsai, S. Chern, 2008, Fertility and sterility.

Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia

Chih-ping Chen, T. Ko, S. Chern, 2005, Prenatal diagnosis.

Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2008, Journal of the Formosan Medical Association = Taiwan yi zhi.

Bowel "dissection" in microvillus inclusion disease.

Chih-ping Chen, C. Hsueh, M. Chiang, 2015, Pediatrics and neonatology.

Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.