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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 2, 2002
Sonographic findings in a case of congenital pyloric diaphragm
C P Chen, J C Sheu, S P Lin, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 25, 2006
Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findings
C P Chen, S P Lin, T Y Chang, 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.
The American Journal of Physiology
|
May 12, 1998
Cis- and trans-acting factors regulating transcription of the BGT1 gene in response to hypertonicity
H Miyakawa, S K Woo, C P Chen, et al.
Journal of Chromatography. A
|
December 19, 2025
Surrogate optimization with multivariate adaptive regression splines for supercritical fluid extraction-supercritical fluid chromatography hyphenated to tandem mass spectrometry
Niray Bhakta, Jaivardhan Sood, Yujing Yang, et al.
The Kaohsiung Journal of Medical Sciences
|
December 31, 1997
Fibroblasts derived from tissue explants of dilantin-induced gingival hyperplasia and idiopathic gingival fibromatosis show distinct disparity in proliferative responsiveness to epidermal growth factor
J S Huang, J K Chen, C P Chen, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 27, 2009
Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations
C P Chen, S R Chern, E J Tsai, et al.
Human Genetics
|
February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes
V Lindgren, C P Chen, C R Bryke, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly
C P Chen, S R Chern, C J Lin, 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 36
Search research articles
Search
Showing results (221-230 of 353) with videos related to
Sort By:
Page
of 36
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 2, 2002
Sonographic findings in a case of congenital pyloric diaphragm
C P Chen, J C Sheu, S P Lin, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 25, 2006
Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findings
C P Chen, S P Lin, T Y Chang, 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.
The American Journal of Physiology
|
May 12, 1998
Cis- and trans-acting factors regulating transcription of the BGT1 gene in response to hypertonicity
H Miyakawa, S K Woo, C P Chen, et al.
Journal of Chromatography. A
|
December 19, 2025
Surrogate optimization with multivariate adaptive regression splines for supercritical fluid extraction-supercritical fluid chromatography hyphenated to tandem mass spectrometry
Niray Bhakta, Jaivardhan Sood, Yujing Yang, et al.
The Kaohsiung Journal of Medical Sciences
|
December 31, 1997
Fibroblasts derived from tissue explants of dilantin-induced gingival hyperplasia and idiopathic gingival fibromatosis show distinct disparity in proliferative responsiveness to epidermal growth factor
J S Huang, J K Chen, C P Chen, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 27, 2009
Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations
C P Chen, S R Chern, E J Tsai, et al.
Human Genetics
|
February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes
V Lindgren, C P Chen, C R Bryke, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly
C P Chen, S R Chern, C J Lin, 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 36