Search filters

List of works by Chin-Yuan Tzen

A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys

scientific article published on 19 November 2008

Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature

scientific article published in October 2004

Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.

scientific article published on January 2004

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

scientific article published on 01 October 2007

Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy

scientific article published on 01 July 2005

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

scientific article published on 01 August 2006

Prenatal diagnosis of de novo terminal deletion of chromosome 7q

scientific article published on May 1, 2003

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction

scientific article published on 01 January 2003

Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly

scientific article published on 01 January 2007

Prenatal diagnosis of pure distal 18q deletion

scientific article published on 01 February 2006

Prenatal diagnosis of the distal 11q deletion and review of the literature

scientific article published on February 2004

Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY)

scientific article published on 01 March 2007

Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion

scientific article

Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13

scientific article published on 01 March 2008

Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings

scientific article published on 01 August 2002

Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature

scientific article published in June 2004