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M Bobrow

Showing results (161-170 of 235) with videos related to

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Prenatal Diagnosis|October 4, 2000
Numbers or words? A randomized controlled trial of presenting screen negative results to pregnant womenT M Marteau, G Saidi, S Goodburn, et al.
Genomics|May 1, 1989
A method for generating hybrids containing nonselected fragments of human chromosomesF Benham, K Hart, J Crolla, et al.
Lancet (London, England)|December 22, 1990
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNAR G Roberts, D R Bentley, T F Barby, et al.
Journal of Public Health Medicine|January 29, 1999
Objectives of genetic counselling: differing views of purchasers, providers and usersS Michie, A Allanson, D Armstrong, et al.
Annals of Human Genetics|October 1, 1977
Assignment of the DIA1 locus to chromosome 22R A Fisher, S Povey, M Bobrow, et al.
BMJ (Clinical Research Ed.)|June 12, 1993
Uptake of cystic fibrosis testing in primary care: supply push or demand pull?H Bekker, M Modell, G Denniss, et al.
Journal of Medical Genetics|March 1, 1991
Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish populationE C Landels, I H Ellis, A H Fensom, et al.
Nucleic Acids Research|October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin geneS C Yau, R G Roberts, D R Bentley, et al.
Journal of Medical Genetics|August 1, 1992
Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British IslesE C Landels, P M Green, I H Ellis, et al.
Journal of Medical Genetics|June 7, 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.
Pageof 24

Showing results (161-170 of 235) with videos related to

Sort By:
Pageof 24
Prenatal Diagnosis|October 4, 2000
Numbers or words? A randomized controlled trial of presenting screen negative results to pregnant womenT M Marteau, G Saidi, S Goodburn, et al.
Genomics|May 1, 1989
A method for generating hybrids containing nonselected fragments of human chromosomesF Benham, K Hart, J Crolla, et al.
Lancet (London, England)|December 22, 1990
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNAR G Roberts, D R Bentley, T F Barby, et al.
Journal of Public Health Medicine|January 29, 1999
Objectives of genetic counselling: differing views of purchasers, providers and usersS Michie, A Allanson, D Armstrong, et al.
Annals of Human Genetics|October 1, 1977
Assignment of the DIA1 locus to chromosome 22R A Fisher, S Povey, M Bobrow, et al.
BMJ (Clinical Research Ed.)|June 12, 1993
Uptake of cystic fibrosis testing in primary care: supply push or demand pull?H Bekker, M Modell, G Denniss, et al.
Journal of Medical Genetics|March 1, 1991
Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish populationE C Landels, I H Ellis, A H Fensom, et al.
Nucleic Acids Research|October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin geneS C Yau, R G Roberts, D R Bentley, et al.
Journal of Medical Genetics|August 1, 1992
Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British IslesE C Landels, P M Green, I H Ellis, et al.
Journal of Medical Genetics|June 7, 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.
Pageof 24