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American Journal of Medical Genetics
|
August 8, 1997
Frequency of associated anomalies in congenital hypoplasia of depressor anguli oris muscle: a study of 50 patients
D S Lin, F Y Huang, S P Lin, et al.
Human Mutation
|
November 26, 1999
Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan
C H Tsai, F J Tsai, J Y Wu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
September 12, 2001
A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan
W D Lin, J Y Wu, C C Lai, et al.
Food Chemistry
|
December 4, 2013
Potential modulation on P-glycoprotein and CYP3A by soymilk and miso: in vivo and ex-vivo studies
C P Yu, Y W Hsieh, S P Lin, et al.
Applied Optics
|
September 11, 2010
Shift-invariant photorefractive joint-transform correlator using Fe:LiNbO(3). crystal plates
Q B He, P Yeh, L J Hu, et al.
Journal of Medical Genetics
|
February 12, 2002
Identification and characterisation of mutations underlying Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)
G J Lee-Chen, S P Lin, S Z Lin, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 11, 2012
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations
C-P Chen, H-M Lin, C Leung, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 25, 2006
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)
C P Chen, S P Lin, C C Lin, et al.
Experimental and Clinical Immunogenetics
|
July 19, 2000
Polymorphism of transmembrane region of MICA gene and Kawasaki disease
Y Huang, Y J Lee, M R Chen, 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 puberty
C P Chen, S P Lin, Y N Su, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 191) with videos related to
Sort By:
Page
of 20
American Journal of Medical Genetics
|
August 8, 1997
Frequency of associated anomalies in congenital hypoplasia of depressor anguli oris muscle: a study of 50 patients
D S Lin, F Y Huang, S P Lin, et al.
Human Mutation
|
November 26, 1999
Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan
C H Tsai, F J Tsai, J Y Wu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
September 12, 2001
A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan
W D Lin, J Y Wu, C C Lai, et al.
Food Chemistry
|
December 4, 2013
Potential modulation on P-glycoprotein and CYP3A by soymilk and miso: in vivo and ex-vivo studies
C P Yu, Y W Hsieh, S P Lin, et al.
Applied Optics
|
September 11, 2010
Shift-invariant photorefractive joint-transform correlator using Fe:LiNbO(3). crystal plates
Q B He, P Yeh, L J Hu, et al.
Journal of Medical Genetics
|
February 12, 2002
Identification and characterisation of mutations underlying Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)
G J Lee-Chen, S P Lin, S Z Lin, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 11, 2012
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations
C-P Chen, H-M Lin, C Leung, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 25, 2006
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)
C P Chen, S P Lin, C C Lin, et al.
Experimental and Clinical Immunogenetics
|
July 19, 2000
Polymorphism of transmembrane region of MICA gene and Kawasaki disease
Y Huang, Y J Lee, M R Chen, 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 puberty
C P Chen, S P Lin, Y N Su, et al.
Page
of 20