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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)|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.
Spine|November 9, 2019
Effects of Surface Topography and Chemistry on Polyether-Ether-Ketone (PEEK) and Titanium OsseointegrationF Brennan Torstrick, Angela S P Lin, David L Safranski, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2022
Leafy and weedy seadragon genomes connect genic and repetitive DNA features to the extravagant biology of syngnathid fishesClayton M Small, Hope M Healey, Mark C Currey, et al.
The American Journal of Pathology|July 25, 2009
Rescue of impaired fracture healing in COX-2-/- mice via activation of prostaglandin E2 receptor subtype 4Chao Xie, Bojian Liang, Ming Xue, 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.
Tissue Engineering. Part A|August 22, 2025
Oxygenation and Temperature Conditioning Alter the Vascular Morphology of Microvascular ConstructsSamuel Nightheart, Adam Rauff, Ethan Dinh, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|September 12, 2001
Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutationsF J Tsai, C C Lee, M C Wu, et al.
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