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S C Finley

Showing results (21-30 of 47) with videos related to

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Journal of Medical Genetics|June 1, 1984
An unbalanced (6q;13q) translocation in a male with clinical features of Ehlers-Danlos type II syndromeP R Scarbrough, J Daw, A J Carroll, et al.
Birth Defects Original Article Series|January 1, 1975
Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndromeJ N Thompson, S C Finley, A E Lorincz, et al.
American Journal of Medical Genetics|October 23, 1997
CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: report and reviewD C Chu, S C Finley, D W Young, et al.
JAMA|November 28, 1977
Participants' reaction to amniocentesis and prenatal genetic studiesS C Finley, P D Varner, P C Vinson, et al.
Journal of Medical Genetics|December 1, 1984
Paternal Robertsonian translocation t(13q;14q) and maternal reciprocal translocation t(7p;13q) in a couple with repeated fetal lossP R Scarbrough, A J Carroll, J B Younger, et al.
The Journal of Pediatrics|October 1, 1972
Triploidy in a live-born male infantW H Finley, S C Finley, M B Green, et al.
Human Genetics|January 1, 1985
High resolution cytogenetic evaluation of couples with recurring fetal wastageT L Yang-Feng, S C Finley, W H Finley, et al.
Behavior Genetics|March 1, 1973
Prison survey for the XYY karyotype in tall inmatesW H Finley, C E McDanal, S C Finley, et al.
American Journal of Diseases of Children (1960)|August 1, 1981
Ring 4 chromosome with terminal p and q deletionsW H Finley, S C Finley, T Chonmaitree, et al.
Clinical Genetics|January 1, 1972
Rheumatoid arthritis in the 46, XX, 18p- syndromeS C Finley, W H Finléy, J C Johnson, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|June 1, 1984
An unbalanced (6q;13q) translocation in a male with clinical features of Ehlers-Danlos type II syndromeP R Scarbrough, J Daw, A J Carroll, et al.
Birth Defects Original Article Series|January 1, 1975
Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndromeJ N Thompson, S C Finley, A E Lorincz, et al.
American Journal of Medical Genetics|October 23, 1997
CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: report and reviewD C Chu, S C Finley, D W Young, et al.
JAMA|November 28, 1977
Participants' reaction to amniocentesis and prenatal genetic studiesS C Finley, P D Varner, P C Vinson, et al.
Journal of Medical Genetics|December 1, 1984
Paternal Robertsonian translocation t(13q;14q) and maternal reciprocal translocation t(7p;13q) in a couple with repeated fetal lossP R Scarbrough, A J Carroll, J B Younger, et al.
The Journal of Pediatrics|October 1, 1972
Triploidy in a live-born male infantW H Finley, S C Finley, M B Green, et al.
Human Genetics|January 1, 1985
High resolution cytogenetic evaluation of couples with recurring fetal wastageT L Yang-Feng, S C Finley, W H Finley, et al.
Behavior Genetics|March 1, 1973
Prison survey for the XYY karyotype in tall inmatesW H Finley, C E McDanal, S C Finley, et al.
American Journal of Diseases of Children (1960)|August 1, 1981
Ring 4 chromosome with terminal p and q deletionsW H Finley, S C Finley, T Chonmaitree, et al.
Clinical Genetics|January 1, 1972
Rheumatoid arthritis in the 46, XX, 18p- syndromeS C Finley, W H Finléy, J C Johnson, et al.
Pageof 5