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S P Lin

Showing results (91-100 of 191) with videos related to

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Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 geneC-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 IIIC 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 administrationJ 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 samplingF 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 systemY 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.
Human Mutation|February 6, 1998
Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndromeF J Tsai, W L Hwu, S P Lin, et al.
Pageof 20

Showing results (91-100 of 191) with videos related to

Sort By:
Pageof 20
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 geneC-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 IIIC 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 administrationJ 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 samplingF 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 systemY 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.
Human Mutation|February 6, 1998
Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndromeF J Tsai, W L Hwu, S P Lin, et al.
Pageof 20