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J C Barber

Showing results (51-60 of 63) with videos related to

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American Journal of Medical Genetics|March 1, 1996
Unbalanced translocation in a mother and her son in one of two 5;10 translocation familiesJ C Barber, I K Temple, P L Campbell, et al.
American Journal of Medical Genetics|December 1, 1994
Small terminal deletions of the long arm of chromosome 2: two new casesA M Fisher, K H Ellis, C E Browne, et al.
British Journal of Haematology|April 1, 1995
t(8;21) myelodysplasia, an early presentation of M2 AMLA S Taj, F M Ross, M Vickers, et al.
Journal of Medical Genetics|April 1, 1997
RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37M M Power, R S James, J C Barber, et al.
Journal of Medical Genetics|February 1, 1993
Identification of the FRAXE fragile site in two families ascertained for X linked mental retardationG A Flynn, M C Hirst, S J Knight, et al.
Current Eye Research|March 1, 1985
Virus-specific, early appearing neutralizing activity and interferon in tears of patients with acute hemorrhagic conjunctivitisM P Langford, J C Barber, V E Sklar, et al.
Prenatal Diagnosis|July 1, 1996
Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samplesA M Fisher, A E Cockwell, K J Moore, et al.
The Journal of Pediatrics|July 1, 1996
Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective studyS A Webber, E Hatchwell, J C Barber, et al.
Human Molecular Genetics|August 1, 1996
Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23I K Temple, R J Gardner, D O Robinson, et al.
Chromosoma|August 20, 1997
Centromeric inactivation in a dicentric human Y;21 translocation chromosomeA M Fisher, L Al-Gazali, T Pramathan, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|March 1, 1996
Unbalanced translocation in a mother and her son in one of two 5;10 translocation familiesJ C Barber, I K Temple, P L Campbell, et al.
American Journal of Medical Genetics|December 1, 1994
Small terminal deletions of the long arm of chromosome 2: two new casesA M Fisher, K H Ellis, C E Browne, et al.
British Journal of Haematology|April 1, 1995
t(8;21) myelodysplasia, an early presentation of M2 AMLA S Taj, F M Ross, M Vickers, et al.
Journal of Medical Genetics|April 1, 1997
RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37M M Power, R S James, J C Barber, et al.
Journal of Medical Genetics|February 1, 1993
Identification of the FRAXE fragile site in two families ascertained for X linked mental retardationG A Flynn, M C Hirst, S J Knight, et al.
Current Eye Research|March 1, 1985
Virus-specific, early appearing neutralizing activity and interferon in tears of patients with acute hemorrhagic conjunctivitisM P Langford, J C Barber, V E Sklar, et al.
Prenatal Diagnosis|July 1, 1996
Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samplesA M Fisher, A E Cockwell, K J Moore, et al.
The Journal of Pediatrics|July 1, 1996
Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective studyS A Webber, E Hatchwell, J C Barber, et al.
Human Molecular Genetics|August 1, 1996
Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23I K Temple, R J Gardner, D O Robinson, et al.
Chromosoma|August 20, 1997
Centromeric inactivation in a dicentric human Y;21 translocation chromosomeA M Fisher, L Al-Gazali, T Pramathan, et al.
Pageof 7