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M Bobrow

Showing results (171-180 of 235) with videos related to

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Journal of Medical Genetics|November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophyS Hodgson, K Hart, S Abbs, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Reinvestigation of two X/autosome translocations:segregation in cell hybridsP L Pearson, W F Witterland, P Meera Khan, et al.
Journal of Medical Genetics|December 1, 1986
Linkage studies in Duchenne and Becker muscular dystrophiesA Walker, K Hart, C Cole, et al.
Journal of Medical Genetics|July 5, 2005
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)J L Whittaker, C Mattocks, D Baralle, et al.
Nucleic Acids Research|January 25, 1989
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophyR G Roberts, C G Cole, K A Hart, et al.
Clinical Genetics|October 1, 1988
PRUFILE: a clinical and laboratory database for the genetics centreD E Mutton, K Chown, L Thomson, et al.
American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.
Prenatal Diagnosis|July 1, 1988
Chromosome banding in direct preparations of chorionic villiM Murer-Orlando, J Llerena, M McGuire, et al.
Tissue Antigens|May 1, 1975
The search for a human equivalent of the mouse T-locus - negative results from a study of HL-A types in spina bifidaM Bobrow, J G Bodmer, W F Bodmer, et al.
Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.
Pageof 24

Showing results (171-180 of 235) with videos related to

Sort By:
Pageof 24
Journal of Medical Genetics|November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophyS Hodgson, K Hart, S Abbs, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Reinvestigation of two X/autosome translocations:segregation in cell hybridsP L Pearson, W F Witterland, P Meera Khan, et al.
Journal of Medical Genetics|December 1, 1986
Linkage studies in Duchenne and Becker muscular dystrophiesA Walker, K Hart, C Cole, et al.
Journal of Medical Genetics|July 5, 2005
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)J L Whittaker, C Mattocks, D Baralle, et al.
Nucleic Acids Research|January 25, 1989
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophyR G Roberts, C G Cole, K A Hart, et al.
Clinical Genetics|October 1, 1988
PRUFILE: a clinical and laboratory database for the genetics centreD E Mutton, K Chown, L Thomson, et al.
American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.
Prenatal Diagnosis|July 1, 1988
Chromosome banding in direct preparations of chorionic villiM Murer-Orlando, J Llerena, M McGuire, et al.
Tissue Antigens|May 1, 1975
The search for a human equivalent of the mouse T-locus - negative results from a study of HL-A types in spina bifidaM Bobrow, J G Bodmer, W F Bodmer, et al.
Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.
Pageof 24