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

M G BUTLER

Showing results (121-130 of 165) with videos related to

Pageof 17
Sort By:
Journal of Gerontology|March 1, 1983
A longitudinal study of nutritional intake in menV K Elahi, D Elahi, R Andres, et al.
Human Molecular Genetics|April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patientY Sun, R D Nicholls, M G Butler, et al.
Journal of Medical Genetics|March 19, 2002
Omphalocele in three generations with autosomal dominant transmissionS L Kanagawa, M L Begleiter, D J Ostlie, et al.
American Journal of Human Genetics|August 1, 1989
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5J Overhauser, U Bengtsson, J McMahon, et al.
American Journal of Medical Genetics|January 1, 1991
An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor geneE W Roback, A J Barakat, V G Dev, et al.
American Journal of Medical Genetics|December 1, 1988
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosisM G Butler, V G Dev, D Shah, et al.
The British Journal of Ophthalmology|August 1, 1992
Fibronectin synthesis in subretinal membranes of proliferative vitreoretinopathyP Hiscott, H A Waller, I Grierson, et al.
American Journal of Medical Genetics|May 8, 2000
Metacarpophalangeal pattern profile analysis in Noonan syndromeM G Butler, R Kumar, M F Davis, et al.
Radiology|July 1, 1995
Meniscal ossicle: radiographic and MR imaging findingsP Schnarkowski, P F Tirman, K D Fuchigami, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
Pageof 17

Showing results (121-130 of 165) with videos related to

Sort By:
Pageof 17
Journal of Gerontology|March 1, 1983
A longitudinal study of nutritional intake in menV K Elahi, D Elahi, R Andres, et al.
Human Molecular Genetics|April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patientY Sun, R D Nicholls, M G Butler, et al.
Journal of Medical Genetics|March 19, 2002
Omphalocele in three generations with autosomal dominant transmissionS L Kanagawa, M L Begleiter, D J Ostlie, et al.
American Journal of Human Genetics|August 1, 1989
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5J Overhauser, U Bengtsson, J McMahon, et al.
American Journal of Medical Genetics|January 1, 1991
An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor geneE W Roback, A J Barakat, V G Dev, et al.
American Journal of Medical Genetics|December 1, 1988
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosisM G Butler, V G Dev, D Shah, et al.
The British Journal of Ophthalmology|August 1, 1992
Fibronectin synthesis in subretinal membranes of proliferative vitreoretinopathyP Hiscott, H A Waller, I Grierson, et al.
American Journal of Medical Genetics|May 8, 2000
Metacarpophalangeal pattern profile analysis in Noonan syndromeM G Butler, R Kumar, M F Davis, et al.
Radiology|July 1, 1995
Meniscal ossicle: radiographic and MR imaging findingsP Schnarkowski, P F Tirman, K D Fuchigami, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
Pageof 17