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B C Davison

Showing results (1-10 of 12) with videos related to

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The Practitioner|September 1, 1981
Genetic counselling and obstetricsB C Davison
Journal of Biosocial Science|October 1, 1973
Genetic counselingB C Davison
Journal of Medical Genetics|March 1, 1970
t(2q-; Dq+) in a mentally retarded female childB C Davison, J Bedford, W Dunn
Journal of Medical Genetics|July 1, 1996
An autosomal dominant syndrome of renal and anogenital malformations with syndactylyA J Green, R N Sandford, B C Davison
American Journal of Medical Genetics|July 1, 1990
Trisomy 20q caused by der (X)t(X;20)(q28;q11.2)J J Waters, D S Gourley, D A Aitken, et al.
American Journal of Medical Genetics|January 1, 1985
X-linked dominant chondrodysplasia punctata: a case report and family studiesR F Mueller, P M Crowle, R A Jones, et al.
Human Molecular Genetics|October 1, 1993
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberD C Rubinsztein, D E Barton, B C Davison, et al.
The British Journal of Ophthalmology|February 1, 1991
Flecked retina associated with ring 17 chromosomeS J Charles, A T Moore, B C Davison, et al.
Lancet (London, England)|December 11, 1971
Contribution of fetal/maternal incompatibility to aetiology of pre-eclamptic toxaemiaA C Stevenson, B C Davison, B Say, et al.
Journal of Medical Genetics|December 1, 1990
Alagille syndrome and deletion of 20pF Anad, J Burn, D Matthews, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Practitioner|September 1, 1981
Genetic counselling and obstetricsB C Davison
Journal of Biosocial Science|October 1, 1973
Genetic counselingB C Davison
Journal of Medical Genetics|March 1, 1970
t(2q-; Dq+) in a mentally retarded female childB C Davison, J Bedford, W Dunn
Journal of Medical Genetics|July 1, 1996
An autosomal dominant syndrome of renal and anogenital malformations with syndactylyA J Green, R N Sandford, B C Davison
American Journal of Medical Genetics|July 1, 1990
Trisomy 20q caused by der (X)t(X;20)(q28;q11.2)J J Waters, D S Gourley, D A Aitken, et al.
American Journal of Medical Genetics|January 1, 1985
X-linked dominant chondrodysplasia punctata: a case report and family studiesR F Mueller, P M Crowle, R A Jones, et al.
Human Molecular Genetics|October 1, 1993
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberD C Rubinsztein, D E Barton, B C Davison, et al.
The British Journal of Ophthalmology|February 1, 1991
Flecked retina associated with ring 17 chromosomeS J Charles, A T Moore, B C Davison, et al.
Lancet (London, England)|December 11, 1971
Contribution of fetal/maternal incompatibility to aetiology of pre-eclamptic toxaemiaA C Stevenson, B C Davison, B Say, et al.
Journal of Medical Genetics|December 1, 1990
Alagille syndrome and deletion of 20pF Anad, J Burn, D Matthews, et al.
Pageof 2