C-P Chen - JoVE Visualize

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Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]|November 6, 2018

[Study on the mechanism of serotype conversion of historical isolates of <i>Shigella flexneri</i>]X Xu, J C Shi, C E Wang, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocationC-P Chen, S-P Lin, C-H Hsu, et al.

European Journal of Medical Genetics|June 14, 2006

24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphismC-P Chen, T-H Wang, S-P Lin, et al.

Pediatric Cardiology|September 18, 2007

Association of vascular endothelial growth factor C-634 g polymorphism in taiwanese children with Kawasaki diseaseK-C Hsueh, Y-J Lin, J-S Chang, et al.

Environmental and Molecular Mutagenesis|June 26, 2001

Gender difference in DNA adduct levels among nonsmoking lung cancer patientsY W Cheng, L L Hsieh, P P Lin, et al.

Genetic Counseling (Geneva, Switzerland)|May 23, 2007

Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)C P Chen, S P Lin, C Y Tzen, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactylyC-P Chen, S-P Lin, M-R Chen, et al.

Prenatal Diagnosis|May 22, 2001

Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesisC P Chen, S R Chern, W Wang, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.

International Journal of Cancer|September 25, 2003

High frequency of activated K-ras codon 15 mutant in colorectal carcinomas from Taiwanese patientsJaw-Yuan Wang, Jan-Sing Hsieh, Fang-Ming Chen, et al.

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Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]|November 6, 2018

[Study on the mechanism of serotype conversion of historical isolates of <i>Shigella flexneri</i>]X Xu, J C Shi, C E Wang, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocationC-P Chen, S-P Lin, C-H Hsu, et al.

European Journal of Medical Genetics|June 14, 2006

24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphismC-P Chen, T-H Wang, S-P Lin, et al.

Pediatric Cardiology|September 18, 2007

Association of vascular endothelial growth factor C-634 g polymorphism in taiwanese children with Kawasaki diseaseK-C Hsueh, Y-J Lin, J-S Chang, et al.

Environmental and Molecular Mutagenesis|June 26, 2001

Gender difference in DNA adduct levels among nonsmoking lung cancer patientsY W Cheng, L L Hsieh, P P Lin, et al.

Genetic Counseling (Geneva, Switzerland)|May 23, 2007

Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)C P Chen, S P Lin, C Y Tzen, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactylyC-P Chen, S-P Lin, M-R Chen, et al.

Prenatal Diagnosis|May 22, 2001

Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesisC P Chen, S R Chern, W Wang, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.

International Journal of Cancer|September 25, 2003

High frequency of activated K-ras codon 15 mutant in colorectal carcinomas from Taiwanese patientsJaw-Yuan Wang, Jan-Sing Hsieh, Fang-Ming Chen, et al.

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