Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P L Wilmot

Showing results (1-10 of 27) with videos related to

Pageof 3
Sort By:
Progress in Clinical and Biological Research|January 1, 1991
Review of cytogenetic data for fragile X detection: lymphocytes and other tissuesP L Wilmot
American Journal of Medical Genetics|January 1, 1986
Prenatal diagnosis of the fra(X) syndromeL R Shapiro, P L Wilmot
Genetics|June 1, 1972
Carbonic anhydrase polymorphism in a New Jersey population of the white-footed mouse Peromyscus leucopusP L Wilmot, D K Underhill
Pediatric Annals|May 1, 1993
Cytogenetic diagnosis of genetic diseasesL R Shapiro, P L Wilmot
The Journal of Heredity|January 1, 1973
Genetic control of two esterase enzymes in Peromyscus leucopusP L Wilmot, D K Underhill
American Journal of Medical Genetics|April 1, 1992
Prenatal cytogenetic diagnosis of the fragile X chromosome: feasibility and speed of in situ clonal method in amniotic fluid cell tissue cultureL R Shapiro, P L Wilmot, L E Andree
American Journal of Medical Genetics|April 1, 1992
Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studiesP D Murphy, P L Wilmot, L R Shapiro
Clinical Genetics|August 1, 1990
Disomic balanced reciprocal translocationP L Wilmot, L R Shapiro, A C Casamassima
American Journal of Medical Genetics|April 1, 1992
Prenatal cytogenetic diagnosis of the fragile X syndrome in amniotic fluid: calculation of accuracyL R Shapiro, P L Wilmot, G S Fisch
American Journal of Medical Genetics|February 1, 1991
Prenatal diagnosis of the fragile X syndrome: possible end of the experimental phase for amniotic fluidL R Shapiro, P L Wilmot, P D Murphy
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Progress in Clinical and Biological Research|January 1, 1991
Review of cytogenetic data for fragile X detection: lymphocytes and other tissuesP L Wilmot
American Journal of Medical Genetics|January 1, 1986
Prenatal diagnosis of the fra(X) syndromeL R Shapiro, P L Wilmot
Genetics|June 1, 1972
Carbonic anhydrase polymorphism in a New Jersey population of the white-footed mouse Peromyscus leucopusP L Wilmot, D K Underhill
Pediatric Annals|May 1, 1993
Cytogenetic diagnosis of genetic diseasesL R Shapiro, P L Wilmot
The Journal of Heredity|January 1, 1973
Genetic control of two esterase enzymes in Peromyscus leucopusP L Wilmot, D K Underhill
American Journal of Medical Genetics|April 1, 1992
Prenatal cytogenetic diagnosis of the fragile X chromosome: feasibility and speed of in situ clonal method in amniotic fluid cell tissue cultureL R Shapiro, P L Wilmot, L E Andree
American Journal of Medical Genetics|April 1, 1992
Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studiesP D Murphy, P L Wilmot, L R Shapiro
Clinical Genetics|August 1, 1990
Disomic balanced reciprocal translocationP L Wilmot, L R Shapiro, A C Casamassima
American Journal of Medical Genetics|April 1, 1992
Prenatal cytogenetic diagnosis of the fragile X syndrome in amniotic fluid: calculation of accuracyL R Shapiro, P L Wilmot, G S Fisch
American Journal of Medical Genetics|February 1, 1991
Prenatal diagnosis of the fragile X syndrome: possible end of the experimental phase for amniotic fluidL R Shapiro, P L Wilmot, P D Murphy
Pageof 3