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P W Thompson
S H Roberts
S M Rees

Human genetics

Showing results (1-10 of 8) with videos related to

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Human Genetics|March 1, 1990
Replication studies in the 16p+ variantP W Thompson, S H Roberts, S M Rees
Human Genetics|May 1, 1987
A new variant of chromosome 16P W Thompson, S H Roberts
Human Genetics|January 1, 1981
Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literatureD P Duckett, S H Roberts
Human Genetics|January 1, 1984
Unbalanced reciprocal translocations in cases of Prader-Willi syndromeD P Duckett, S H Roberts, P Davies
Human Genetics|February 1, 1987
Homozygous paracentric inversion 12 in a mentally retarded boy: a case report and review of the literatureH A Price, S H Roberts, K M Laurence
Human Genetics|May 1, 1993
Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12M Upadhyaya, S H Roberts, J Farnham, et al.
Human Genetics|January 1, 1985
Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qterM Worwood, J D Brook, S J Cragg, et al.
Human Genetics|May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessmentsJ D Brook, S J Knight, S H Roberts, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human Genetics|March 1, 1990
Replication studies in the 16p+ variantP W Thompson, S H Roberts, S M Rees
Human Genetics|May 1, 1987
A new variant of chromosome 16P W Thompson, S H Roberts
Human Genetics|January 1, 1981
Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literatureD P Duckett, S H Roberts
Human Genetics|January 1, 1984
Unbalanced reciprocal translocations in cases of Prader-Willi syndromeD P Duckett, S H Roberts, P Davies
Human Genetics|February 1, 1987
Homozygous paracentric inversion 12 in a mentally retarded boy: a case report and review of the literatureH A Price, S H Roberts, K M Laurence
Human Genetics|May 1, 1993
Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12M Upadhyaya, S H Roberts, J Farnham, et al.
Human Genetics|January 1, 1985
Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qterM Worwood, J D Brook, S J Cragg, et al.
Human Genetics|May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessmentsJ D Brook, S J Knight, S H Roberts, et al.
Pageof 1