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S M Huson

Showing results (71-80 of 85) with videos related to

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Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.
British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Lancet (London, England)|June 10, 1998
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancyC H Gonzalez, M J Marques-Dias, C A Kim, et al.
Archives of Disease in Childhood|January 1, 1995
DNA testing for fragile X syndrome in schools for learning difficultiesS F Slaney, A O Wilkie, M C Hirst, et al.
American Journal of Medical Genetics|June 15, 1993
Complete and partial XY sex reversal associated with terminal deletion of 10q: report of 2 cases and literature reviewA O Wilkie, F M Campbell, P Daubeney, et al.
Journal of Medical Genetics|May 16, 2009
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeG Spurlock, E Bennett, N Chuzhanova, et al.
American Journal of Medical Genetics|May 8, 2000
Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotypeL A Brueton, S M Huson, P M Cox, et al.
Nature|February 8, 1990
Paternal origin of new mutations in von Recklinghausen neurofibromatosisD Jadayel, P Fain, M Upadhyaya, et al.
American Journal of Medical Genetics|April 1, 1992
Molecular studies of the fragile X syndromeS J Knight, M C Hirst, A Roche, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.
British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Lancet (London, England)|June 10, 1998
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancyC H Gonzalez, M J Marques-Dias, C A Kim, et al.
Archives of Disease in Childhood|January 1, 1995
DNA testing for fragile X syndrome in schools for learning difficultiesS F Slaney, A O Wilkie, M C Hirst, et al.
American Journal of Medical Genetics|June 15, 1993
Complete and partial XY sex reversal associated with terminal deletion of 10q: report of 2 cases and literature reviewA O Wilkie, F M Campbell, P Daubeney, et al.
Journal of Medical Genetics|May 16, 2009
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeG Spurlock, E Bennett, N Chuzhanova, et al.
American Journal of Medical Genetics|May 8, 2000
Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotypeL A Brueton, S M Huson, P M Cox, et al.
Nature|February 8, 1990
Paternal origin of new mutations in von Recklinghausen neurofibromatosisD Jadayel, P Fain, M Upadhyaya, et al.
American Journal of Medical Genetics|April 1, 1992
Molecular studies of the fragile X syndromeS J Knight, M C Hirst, A Roche, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
Pageof 9