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

G S Stephen

Showing results (1-10 of 14) with videos related to

Pageof 2
Sort By:
American Journal of Obstetrics and Gynecology|November 1, 1979
Determination of correct karyotypeG S Stephen
Journal of Medical Genetics|May 1, 1987
Structural rearrangements in the parents of children with primary trisomy 21D A Couzin, J L Watt, G S Stephen
Cancer Genetics and Cytogenetics|July 1, 1986
A possible case of chronic leukoerythroblastosis associated with t(12;14)(p13;q22) in bone marrow cellsD A Couzin, A A Dawson, G S Stephen
Prenatal Diagnosis|January 1, 1986
The prenatal detection of a familial pericentric inversion of chromosome 19D A Couzin, J L Watt, G S Stephen
Journal of Medical Genetics|August 1, 1991
Interstitial deletion of chromosome 13: prognosis and adult phenotypeJ C Dean, S Simpson, D A Couzin, et al.
Prenatal Diagnosis|September 1, 1986
Yet another method for processing trophoblastJ L Watt, J Mackay, G S Stephen, et al.
Prenatal Diagnosis|January 1, 1989
Prenatal diagnosis of a case of 46,XY,18p-/46,XY,18p+ mosaicismG S Stephen, D A Couzin, J L Watt, et al.
Journal of Medical Genetics|August 1, 1986
A paracentric inversion of 7q illustrating a possible interchromosomal effectJ L Watt, K Ward, D A Couzin, et al.
Journal of Medical Genetics|October 1, 1984
A familial insertion involving an active nucleolar organiser within chromosome 12J L Watt, D A Couzin, D J Lloyd, et al.
Clinical Genetics|November 1, 1991
Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental fieldJ C Dean, D A Couzin, E S Gray, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
American Journal of Obstetrics and Gynecology|November 1, 1979
Determination of correct karyotypeG S Stephen
Journal of Medical Genetics|May 1, 1987
Structural rearrangements in the parents of children with primary trisomy 21D A Couzin, J L Watt, G S Stephen
Cancer Genetics and Cytogenetics|July 1, 1986
A possible case of chronic leukoerythroblastosis associated with t(12;14)(p13;q22) in bone marrow cellsD A Couzin, A A Dawson, G S Stephen
Prenatal Diagnosis|January 1, 1986
The prenatal detection of a familial pericentric inversion of chromosome 19D A Couzin, J L Watt, G S Stephen
Journal of Medical Genetics|August 1, 1991
Interstitial deletion of chromosome 13: prognosis and adult phenotypeJ C Dean, S Simpson, D A Couzin, et al.
Prenatal Diagnosis|September 1, 1986
Yet another method for processing trophoblastJ L Watt, J Mackay, G S Stephen, et al.
Prenatal Diagnosis|January 1, 1989
Prenatal diagnosis of a case of 46,XY,18p-/46,XY,18p+ mosaicismG S Stephen, D A Couzin, J L Watt, et al.
Journal of Medical Genetics|August 1, 1986
A paracentric inversion of 7q illustrating a possible interchromosomal effectJ L Watt, K Ward, D A Couzin, et al.
Journal of Medical Genetics|October 1, 1984
A familial insertion involving an active nucleolar organiser within chromosome 12J L Watt, D A Couzin, D J Lloyd, et al.
Clinical Genetics|November 1, 1991
Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental fieldJ C Dean, D A Couzin, E S Gray, et al.
Pageof 2