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Genetic Counseling (Geneva, Switzerland)|April 23, 2005
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephalyC P Chen, S R Chern, C J Lin, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.
Zhonghua Minguo Wei Sheng Wu Ji Mian Yi Xue Za Zhi = Chinese Journal of Microbiology and Immunology|May 1, 1995
Isolation and identification of influenza viruses from clinical materials in 1977-1993 at Veterans General Hospital-TaipeiW T Liu, H Y Wei, S T Hu, et al.
Journal of Medical Genetics|December 24, 1998
De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasiaC P Chen, S R Chern, C C Lee, et al.
Human Reproduction (Oxford, England)|January 22, 1998
Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasiaC P Chen, S R Chern, T Y Wang, et al.
Prenatal Diagnosis|May 29, 1998
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetusC P Chen, S R Chern, C C Lee, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXYC P Chen, S R Chern, C L Chang, et al.
Prenatal Diagnosis|March 10, 2001
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasiaC P Chen, S R Chern, J C Shih, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.
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