S P Lin - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

S P Lin

Showing results (51-60 of 191) with videos related to

Pageof 20

Sort By:

Fetal Diagnosis and Therapy|February 6, 1999

Perinatal findings in a male fetus with congenital megacystis and anorectal malformationsC P Chen, W Wang, S P Lin, et al.

American Journal of Perinatology|March 4, 1999

Favorable outcome in a fetus with an early-onset extensive cystic hygroma colli and intralesional hemorrhageC P Chen, W Wang, S P Lin, et al.

Applied Optics|February 13, 2008

Anisotropy in the absorption and scattering spectra of chicken breast tissueG Marquez, L V Wang, S P Lin, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1-->p23) associated with attention deficit and hyperactivity disorderC-P Chen, S-P Lin, J-W Su, et al.

Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|May 1, 1992

Liveborn trisomy 22: report of one caseS F Lean, S P Lin, E Y Shen, et al.

Human Mutation|March 29, 2000

Identification of a novel missense mutation (T16A) in the glucose-6-phosphatase gene in a Taiwan Chinese patient with glycogen storage disease Ia (Von Gierke disease)M C Wu, F J Tsai, C C Le, et al.

Journal of Assisted Reproduction and Genetics|January 13, 2001

Embryonic dormancy phenomenon in obstructed healthy mouse fallopian tubesR K Lee, S P Lin, Y J Tsai, et al.

Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|November 1, 1990

[Propionic acidemia: report of a case that is successfully managed by peritoneal dialysis and sodium benzoate therapy]W C Hsu, S P Lin, F Y Huang, et al.

Journal of Assisted Reproduction and Genetics|November 21, 1998

Separating X-bearing human spermatozoa through a discontinuous Percoll density gradient proved to be inefficient by double-label fluorescent in situ hybridizationS P Lin, R K Lee, Y J Tsai, et al.

Genetic Counseling (Geneva, Switzerland)|March 23, 2007

An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literatureC B Wang, S P Lin, C P Chen, et al.

Pageof 20

Search research articles

Showing results (51-60 of 191) with videos related to

Sort By:

Pageof 20

Fetal Diagnosis and Therapy|February 6, 1999

Perinatal findings in a male fetus with congenital megacystis and anorectal malformationsC P Chen, W Wang, S P Lin, et al.

American Journal of Perinatology|March 4, 1999

Favorable outcome in a fetus with an early-onset extensive cystic hygroma colli and intralesional hemorrhageC P Chen, W Wang, S P Lin, et al.

Applied Optics|February 13, 2008

Anisotropy in the absorption and scattering spectra of chicken breast tissueG Marquez, L V Wang, S P Lin, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1-->p23) associated with attention deficit and hyperactivity disorderC-P Chen, S-P Lin, J-W Su, et al.

Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|May 1, 1992

Liveborn trisomy 22: report of one caseS F Lean, S P Lin, E Y Shen, et al.

Human Mutation|March 29, 2000

Identification of a novel missense mutation (T16A) in the glucose-6-phosphatase gene in a Taiwan Chinese patient with glycogen storage disease Ia (Von Gierke disease)M C Wu, F J Tsai, C C Le, et al.

Journal of Assisted Reproduction and Genetics|January 13, 2001

Embryonic dormancy phenomenon in obstructed healthy mouse fallopian tubesR K Lee, S P Lin, Y J Tsai, et al.

Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|November 1, 1990

[Propionic acidemia: report of a case that is successfully managed by peritoneal dialysis and sodium benzoate therapy]W C Hsu, S P Lin, F Y Huang, et al.

Journal of Assisted Reproduction and Genetics|November 21, 1998

Separating X-bearing human spermatozoa through a discontinuous Percoll density gradient proved to be inefficient by double-label fluorescent in situ hybridizationS P Lin, R K Lee, Y J Tsai, et al.

Genetic Counseling (Geneva, Switzerland)|March 23, 2007

An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literatureC B Wang, S P Lin, C P Chen, et al.

Pageof 20