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A P Read

Showing results (21-30 of 102) with videos related to

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Journal of Medical Genetics|August 1, 1997
Waardenburg syndromeA P Read, V E Newton
The British Journal of Ophthalmology|January 1, 1992
Is there a genetic basis for Fuchs' heterochromic uveitis? Discordance in monozygotic twinsN P Jones, A P Read
Journal of Medical Genetics|February 1, 1988
Norrie disease resulting from a gene deletion: clinical features and DNA studiesD Donnai, R C Mountford, A P Read
Journal of Medical Genetics|September 1, 1992
Beckwith-Wiedemann syndromeA M Norman, A P Read, D Donnai
Nature Genetics|November 1, 1994
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) geneM Tassabehji, V E Newton, A P Read
Journal of Medical Genetics|April 1, 1989
Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA bankingJ R Yates, S Malcolm, A P Read
American Journal of Medical Genetics|February 15, 1992
Monozygotic twinning and Wiedemann-Beckwith syndromeJ Clayton-Smith, A P Read, D Donnai
Lancet (London, England)|February 7, 1981
False positive results with the qualitative amniotic fluid acetylcholinesterase testA P Read, S J Fennell, D Donnai
Journal of Medical Genetics|December 1, 1988
Hypomelanosis of Ito: a manifestation of mosaicism or chimerismD Donnai, A P Read, C McKeown, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Localization of a gene for Waardenburg syndrome type IA P Read, C Foy, V Newton, et al.
Pageof 11

Showing results (21-30 of 102) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|August 1, 1997
Waardenburg syndromeA P Read, V E Newton
The British Journal of Ophthalmology|January 1, 1992
Is there a genetic basis for Fuchs' heterochromic uveitis? Discordance in monozygotic twinsN P Jones, A P Read
Journal of Medical Genetics|February 1, 1988
Norrie disease resulting from a gene deletion: clinical features and DNA studiesD Donnai, R C Mountford, A P Read
Journal of Medical Genetics|September 1, 1992
Beckwith-Wiedemann syndromeA M Norman, A P Read, D Donnai
Nature Genetics|November 1, 1994
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) geneM Tassabehji, V E Newton, A P Read
Journal of Medical Genetics|April 1, 1989
Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA bankingJ R Yates, S Malcolm, A P Read
American Journal of Medical Genetics|February 15, 1992
Monozygotic twinning and Wiedemann-Beckwith syndromeJ Clayton-Smith, A P Read, D Donnai
Lancet (London, England)|February 7, 1981
False positive results with the qualitative amniotic fluid acetylcholinesterase testA P Read, S J Fennell, D Donnai
Journal of Medical Genetics|December 1, 1988
Hypomelanosis of Ito: a manifestation of mosaicism or chimerismD Donnai, A P Read, C McKeown, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Localization of a gene for Waardenburg syndrome type IA P Read, C Foy, V Newton, et al.
Pageof 11