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J C Barber

Showing results (31-40 of 63) with videos related to

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Survey of Ophthalmology|March 1, 1989
Ocular choristomasA M Mansour, J C Barber, R D Reinecke, et al.
Human Genetics|May 14, 1999
Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic levelJ C Barber, C J Reed, S P Dahoun, et al.
Journal of Medical Genetics|December 1, 1996
Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patientsC A Joyce, B Zorich, S J Pike, et al.
Lancet (London, England)|November 30, 1996
Repeated cytogenetic culture failure as an indicator of immunodeficiencyJ C Barber, J M Walker, M R Barker, et al.
The Journal of Rheumatology|July 1, 1982
Overlap syndrome of juvenile rheumatoid arthritis and systemic lupus erythematosusF T Saulsbury, R W Kesler, J M Kennaugh, et al.
Pediatrics|February 1, 1983
Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generationsJ F Reynolds, J C Barber, B A Alford, et al.
Investigative Ophthalmology & Visual Science|June 1, 1986
Conjunctivitis in rabbits caused by enterovirus type 70 (EV70)M P Langford, M Yin-Murphy, J C Barber, et al.
Clinical Genetics|November 24, 1999
Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalitiesC A Joyce, F M Ross, N R Dennis, et al.
Human Genetics|December 22, 1998
Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15qJ C Barber, I E Cross, F Douglas, et al.
Infection and Immunity|September 1, 1980
Human fibroblast interferon in tears of patients with picornavirus epidemic conjunctivitisM P Langford, M Yin-Murphy, Y M Ho, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Survey of Ophthalmology|March 1, 1989
Ocular choristomasA M Mansour, J C Barber, R D Reinecke, et al.
Human Genetics|May 14, 1999
Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic levelJ C Barber, C J Reed, S P Dahoun, et al.
Journal of Medical Genetics|December 1, 1996
Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patientsC A Joyce, B Zorich, S J Pike, et al.
Lancet (London, England)|November 30, 1996
Repeated cytogenetic culture failure as an indicator of immunodeficiencyJ C Barber, J M Walker, M R Barker, et al.
The Journal of Rheumatology|July 1, 1982
Overlap syndrome of juvenile rheumatoid arthritis and systemic lupus erythematosusF T Saulsbury, R W Kesler, J M Kennaugh, et al.
Pediatrics|February 1, 1983
Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generationsJ F Reynolds, J C Barber, B A Alford, et al.
Investigative Ophthalmology & Visual Science|June 1, 1986
Conjunctivitis in rabbits caused by enterovirus type 70 (EV70)M P Langford, M Yin-Murphy, J C Barber, et al.
Clinical Genetics|November 24, 1999
Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalitiesC A Joyce, F M Ross, N R Dennis, et al.
Human Genetics|December 22, 1998
Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15qJ C Barber, I E Cross, F Douglas, et al.
Infection and Immunity|September 1, 1980
Human fibroblast interferon in tears of patients with picornavirus epidemic conjunctivitisM P Langford, M Yin-Murphy, Y M Ho, et al.
Pageof 7