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Genetic Counseling (Geneva, Switzerland)
|
September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughter
C P Chen, S P Lin, S R Chern, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III
C P Chen, S P Lin, Y N Suo, et al.
AJNR. American Journal of Neuroradiology
|
August 14, 2010
Improvement in angiographic cerebral vasospasm after intra-arterial verapamil administration
J V Sehy, W E Holloway, S-P Lin, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 25, 2001
Galloway-Mowat syndrome: a glomerular basement membrane disorder?
C C Lin, J D Tsai, S P Lin, et al.
Obstetrics and Gynecology
|
January 1, 1995
Limb defects after chorionic villus sampling
F J Hsieh, M K Shyu, B C Sheu, et al.
Human Reproduction (Oxford, England)
|
September 18, 1998
Development of hatching blastocysts from immature human oocytes following in-vitro maturation and fertilization using a co-culture system
Y M Hwu, R K Lee, C P Chen, et al.
Human Genetics
|
March 1, 1997
Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)
H H Lee, J G Chang, S P Lin, et al.
American Journal of Perinatology
|
November 1, 1996
Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome)
C P Chen, S P Lin, F F Liu, et al.
European Journal of Clinical Nutrition
|
October 20, 2005
Negative effect of heat sterilization on the free amino acid concentrations in infant formula
C Y Yeung, H C Lee, S P Lin, et al.
American Journal of Medical Genetics
|
November 1, 1992
Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy
S P Lin, E M Petty, L H Gibson, et al.
Page
of 16
Search research articles
Search
Showing results (71-80 of 154) with videos related to
Sort By:
Page
of 16
Genetic Counseling (Geneva, Switzerland)
|
September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughter
C P Chen, S P Lin, S R Chern, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III
C P Chen, S P Lin, Y N Suo, et al.
AJNR. American Journal of Neuroradiology
|
August 14, 2010
Improvement in angiographic cerebral vasospasm after intra-arterial verapamil administration
J V Sehy, W E Holloway, S-P Lin, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 25, 2001
Galloway-Mowat syndrome: a glomerular basement membrane disorder?
C C Lin, J D Tsai, S P Lin, et al.
Obstetrics and Gynecology
|
January 1, 1995
Limb defects after chorionic villus sampling
F J Hsieh, M K Shyu, B C Sheu, et al.
Human Reproduction (Oxford, England)
|
September 18, 1998
Development of hatching blastocysts from immature human oocytes following in-vitro maturation and fertilization using a co-culture system
Y M Hwu, R K Lee, C P Chen, et al.
Human Genetics
|
March 1, 1997
Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)
H H Lee, J G Chang, S P Lin, et al.
American Journal of Perinatology
|
November 1, 1996
Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome)
C P Chen, S P Lin, F F Liu, et al.
European Journal of Clinical Nutrition
|
October 20, 2005
Negative effect of heat sterilization on the free amino acid concentrations in infant formula
C Y Yeung, H C Lee, S P Lin, et al.
American Journal of Medical Genetics
|
November 1, 1992
Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy
S P Lin, E M Petty, L H Gibson, et al.
Page
of 16