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Prenatal Diagnosis
|
May 23, 2000
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes
C P Chen, K Devriendt, S R Chern, et al.
Arthritis and Rheumatism
|
January 11, 2012
Quantitative imaging of cartilage and bone morphology, reactive oxygen species, and vascularization in a rodent model of osteoarthritis
LiQin Xie, Angela S P Lin, Kousik Kundu, et al.
Journal of Orthopaedic Surgery and Research
|
September 28, 2016
The effect of contouring on fatigue resistance of three types of fracture fixation plates
Angela S P Lin, Chelsea M Fechter, Mark Magill, et al.
Genomics
|
March 1, 1992
Assignment of two human alpha-1,3-galactosyltransferase gene sequences (GGTA1 and GGTA1P) to chromosomes 9q33-q34 and 12q14-q15
N L Shaper, S P Lin, D H Joziasse, et al.
Journal of Biomechanical Engineering
|
July 17, 2009
In vivo model for evaluating the effects of mechanical stimulation on tissue-engineered bone repair
Joel D Boerckel, Kenneth M Dupont, Yash M Kolambkar, et al.
Clinical Genetics
|
March 1, 1995
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family
J Zielenski, D Markiewicz, S P Lin, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 16, 2008
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation
C-P Chen, S-P Lin, Y-N Su, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
September 1, 1988
Effects of prenatal exposure to neuroleptic drugs on children's growth
J E Platt, A J Friedhoff, S H Broman, et al.
The American Journal of Psychiatry
|
December 1, 1996
Schizoid personality disorder after prenatal exposure to famine
H W Hoek, E Susser, K A Buck, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 23, 2012
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome
C P Chen, S P Lin, D S Lin, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 154) with videos related to
Sort By:
Page
of 16
Prenatal Diagnosis
|
May 23, 2000
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes
C P Chen, K Devriendt, S R Chern, et al.
Arthritis and Rheumatism
|
January 11, 2012
Quantitative imaging of cartilage and bone morphology, reactive oxygen species, and vascularization in a rodent model of osteoarthritis
LiQin Xie, Angela S P Lin, Kousik Kundu, et al.
Journal of Orthopaedic Surgery and Research
|
September 28, 2016
The effect of contouring on fatigue resistance of three types of fracture fixation plates
Angela S P Lin, Chelsea M Fechter, Mark Magill, et al.
Genomics
|
March 1, 1992
Assignment of two human alpha-1,3-galactosyltransferase gene sequences (GGTA1 and GGTA1P) to chromosomes 9q33-q34 and 12q14-q15
N L Shaper, S P Lin, D H Joziasse, et al.
Journal of Biomechanical Engineering
|
July 17, 2009
In vivo model for evaluating the effects of mechanical stimulation on tissue-engineered bone repair
Joel D Boerckel, Kenneth M Dupont, Yash M Kolambkar, et al.
Clinical Genetics
|
March 1, 1995
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family
J Zielenski, D Markiewicz, S P Lin, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 16, 2008
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation
C-P Chen, S-P Lin, Y-N Su, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
September 1, 1988
Effects of prenatal exposure to neuroleptic drugs on children's growth
J E Platt, A J Friedhoff, S H Broman, et al.
The American Journal of Psychiatry
|
December 1, 1996
Schizoid personality disorder after prenatal exposure to famine
H W Hoek, E Susser, K A Buck, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 23, 2012
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome
C P Chen, S P Lin, D S Lin, et al.
Page
of 16