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

A J Barnicoat

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

Pageof 1
Sort By:
Developmental Medicine and Child Neurology|June 1, 1993
Where have all the fragile X boys gone?A J Barnicoat, Z Docherty, M Bobrow
Clinical Dysmorphology|October 1, 1994
Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS)A J Barnicoat, M J Seller, C P Bennett
American Journal of Medical Genetics|May 16, 1997
Two sibs with partial trisomy 2qA J Barnicoat, I Abusaad, C M Mackie, et al.
Health Technology Assessment (Winchester, England)|March 23, 2001
An assessment of screening strategies for fragile X syndrome in the UKM E Pembrey, A J Barnicoat, B Carmichael, et al.
Experientia|December 15, 1981
Observations on salicyl hydroxamic acid, an experimental trypanocideA J Barnicoat, W G van't Hoff, P J Morrison, et al.
Journal of Medical Genetics|September 1, 1995
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255C P Bennett, A J Barnicoat, F Cotter, et al.
Journal of Chromatography|September 11, 1981
Determination of salicylhydroxamic acid, a trypanocidal agent, by reversed phase high-performance liquid chromatographyA J Barnicoat, W G van 't Hoff, P J Morrison, et al.
Clinical Dysmorphology|April 1, 1996
An unusual presentation of Smith-Magenis syndrome with iris dysgenesisA J Barnicoat, H U Moller, R W Palmer, et al.
Journal of Medical Genetics|January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXEA J Barnicoat, Q Wang, J Turk, et al.
Clinical Genetics|January 1, 1996
Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: Clinical assessmentA J Barnicoat, J L Bonneau, E Boyd, et al.
Pageof 1

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

Sort By:
Pageof 1
Developmental Medicine and Child Neurology|June 1, 1993
Where have all the fragile X boys gone?A J Barnicoat, Z Docherty, M Bobrow
Clinical Dysmorphology|October 1, 1994
Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS)A J Barnicoat, M J Seller, C P Bennett
American Journal of Medical Genetics|May 16, 1997
Two sibs with partial trisomy 2qA J Barnicoat, I Abusaad, C M Mackie, et al.
Health Technology Assessment (Winchester, England)|March 23, 2001
An assessment of screening strategies for fragile X syndrome in the UKM E Pembrey, A J Barnicoat, B Carmichael, et al.
Experientia|December 15, 1981
Observations on salicyl hydroxamic acid, an experimental trypanocideA J Barnicoat, W G van't Hoff, P J Morrison, et al.
Journal of Medical Genetics|September 1, 1995
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255C P Bennett, A J Barnicoat, F Cotter, et al.
Journal of Chromatography|September 11, 1981
Determination of salicylhydroxamic acid, a trypanocidal agent, by reversed phase high-performance liquid chromatographyA J Barnicoat, W G van 't Hoff, P J Morrison, et al.
Clinical Dysmorphology|April 1, 1996
An unusual presentation of Smith-Magenis syndrome with iris dysgenesisA J Barnicoat, H U Moller, R W Palmer, et al.
Journal of Medical Genetics|January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXEA J Barnicoat, Q Wang, J Turk, et al.
Clinical Genetics|January 1, 1996
Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: Clinical assessmentA J Barnicoat, J L Bonneau, E Boyd, et al.
Pageof 1