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Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay
C 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 translocation
C-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 dysmorphism
C-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 Osseointegration
F 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 fishes
Clayton 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 4
Chao Xie, Bojian Liang, Ming Xue, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 16, 2008
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings
C-P Chen, S-P Lin, F-J Tsai, 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 polydactyly
C-P Chen, S-P Lin, M-R Chen, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
A 5.3-Mb duplication of 9p12 --> p13.1 characterized by array CGH in a female infant with developmental delay
C P Chen, S P Lin, S R Chern, et al.
Page
of 20
Search research articles
Search
Showing results (141-150 of 191) with videos related to
Sort By:
Page
of 20
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay
C 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 translocation
C-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 dysmorphism
C-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 Osseointegration
F 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 fishes
Clayton 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 4
Chao Xie, Bojian Liang, Ming Xue, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 16, 2008
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings
C-P Chen, S-P Lin, F-J Tsai, 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 polydactyly
C-P Chen, S-P Lin, M-R Chen, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
A 5.3-Mb duplication of 9p12 --> p13.1 characterized by array CGH in a female infant with developmental delay
C P Chen, S P Lin, S R Chern, et al.
Page
of 20