Tzu-Jou Wang

NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome

Tom Strachan, M. Bamshad, T. Strachan, 2004, Nature Genetics.

Y-chromosome genes associated with sertoli cell-only syndrome identified by array comparative genome hybridization

Tzu-Jou Wang, Hong-Yo Kang, K. Lan, 2022, Biomedical journal.

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3

I. Krantz, T. Strachan, S. Lindsay, 2004, Human Genetics.

Epignathus Teratoma with Duplication of Mandible and Tongue: Report of a Case

Tzu-Jou Wang, C. Lui, Jui-Pin Lai, 2013, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints

Y. Chien, W. Hwu, Tzu-Jou Wang, 2010, American journal of medical genetics. Part A.

Novel mutation in boy with cartilage-hair hypoplasia.

Tzu-Jou Wang, Hong-Ren Yu, I. Lin, 2010, Pediatrics and neonatology.

Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019)

Y. Chien, W. Hwu, F. Tsai, 2020, Orphanet Journal of Rare Diseases.

Plasma Clusterin Levels in Predicting the Occurrence of Coronary Artery Lesions in Patients With Kawasaki Disease

Kuender D Yang, Tzu-Jou Wang, J. Sheen, 2010, Pediatric Cardiology.

Mutation survey in Taiwanese patients with Stickler syndrome

Pei-Chang Wu, Yi-Hao Chen, Hsi-Kung Kuo, 2022, Taiwan journal of ophthalmology.

Novel mutations of IRF6 gene in Taiwanese Van der Woude syndrome patients.

Tzu-Jou Wang, Meng-Han Tsai, Jui-Pin Lai, 2019, Pediatrics and neonatology.

Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints

Y. Chien, W. Hwu, Tzu-Jou Wang, 2010, American journal of medical genetics. Part A.