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C P Chen

Showing results (301-310 of 353) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 1, 2008
Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidneyC-P Chen, Y-P Liu, J-P Huang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 26, 2003
Prenatal diagnosis of de novo mosaic distal 18q deletion associated with congenital anomaliesC-P Chen, C-Y Tzen, T-Y Chang, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed pubertyC P Chen, S P Lin, Y N Su, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delayC P Chen, S P Lin, Y N Su, et al.
Pediatric Radiology|January 1, 1997
In utero urinary bladder perforation, urinary ascites, and bilateral contained urinomas secondary to posterior urethral valves: clinical and imaging findingsC Chen, S L Shih, F F Liu, et al.
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.
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesisC P Chen, C C Lee, D D Town, 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.
Pageof 36

Showing results (301-310 of 353) with videos related to

Sort By:
Pageof 36
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 1, 2008
Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidneyC-P Chen, Y-P Liu, J-P Huang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 26, 2003
Prenatal diagnosis of de novo mosaic distal 18q deletion associated with congenital anomaliesC-P Chen, C-Y Tzen, T-Y Chang, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed pubertyC P Chen, S P Lin, Y N Su, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delayC P Chen, S P Lin, Y N Su, et al.
Pediatric Radiology|January 1, 1997
In utero urinary bladder perforation, urinary ascites, and bilateral contained urinomas secondary to posterior urethral valves: clinical and imaging findingsC Chen, S L Shih, F F Liu, et al.
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.
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesisC P Chen, C C Lee, D D Town, 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.
Pageof 36