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P S Harper

Showing results (171-180 of 345) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1989
Report of the committee on clinical disorders and chromosomal deletion syndromesP S Harper, J Frézal, M A Ferguson-Smith, et al.
Human Genetics|January 1, 1984
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequencesH M Kingston, M Sarfarazi, N S Thomas, et al.
Lancet (London, England)|October 6, 1984
Chorion biopsy for prenatal testing in Hunter's syndromeP S Harper, S Bamforth, D Rees, et al.
American Journal of Human Genetics|July 1, 1992
Anticipation in myotonic dystrophy: new light on an old problemP S Harper, H G Harley, W Reardon, et al.
Journal of Medical Genetics|December 19, 2001
Eight years' experience of direct molecular testing for myotonic dystrophy in WalesS Fokstuen, J Myring, L Meredith, et al.
Lancet (London, England)|April 10, 1976
Letter: Prenatal prediction of myotonic dystrophyJ Insley, G W Bird, P S Harper, et al.
Journal of Medical Genetics|February 1, 1983
Huntington's chorea in South Wales: mutation, fertility, and genetic fitnessD A Walker, P S Harper, R G Newcombe, et al.
Archives of Disease in Childhood|February 1, 1993
The natural history of congenital myotonic dystrophy: mortality and long term clinical aspectsW Reardon, R Newcombe, I Fenton, et al.
Journal of Medical Genetics|December 1, 1982
A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe formsI D Young, P S Harper, R G Newcombe, et al.
Clinical Genetics|November 1, 1986
Marfan syndrome: exclusion of genetic linkage to the COL1A2 geneP Tsipouras, A L Børresen, S Bamforth, et al.
Pageof 35

Showing results (171-180 of 345) with videos related to

Sort By:
Pageof 35
Cytogenetics and Cell Genetics|January 1, 1989
Report of the committee on clinical disorders and chromosomal deletion syndromesP S Harper, J Frézal, M A Ferguson-Smith, et al.
Human Genetics|January 1, 1984
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequencesH M Kingston, M Sarfarazi, N S Thomas, et al.
Lancet (London, England)|October 6, 1984
Chorion biopsy for prenatal testing in Hunter's syndromeP S Harper, S Bamforth, D Rees, et al.
American Journal of Human Genetics|July 1, 1992
Anticipation in myotonic dystrophy: new light on an old problemP S Harper, H G Harley, W Reardon, et al.
Journal of Medical Genetics|December 19, 2001
Eight years' experience of direct molecular testing for myotonic dystrophy in WalesS Fokstuen, J Myring, L Meredith, et al.
Lancet (London, England)|April 10, 1976
Letter: Prenatal prediction of myotonic dystrophyJ Insley, G W Bird, P S Harper, et al.
Journal of Medical Genetics|February 1, 1983
Huntington's chorea in South Wales: mutation, fertility, and genetic fitnessD A Walker, P S Harper, R G Newcombe, et al.
Archives of Disease in Childhood|February 1, 1993
The natural history of congenital myotonic dystrophy: mortality and long term clinical aspectsW Reardon, R Newcombe, I Fenton, et al.
Journal of Medical Genetics|December 1, 1982
A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe formsI D Young, P S Harper, R G Newcombe, et al.
Clinical Genetics|November 1, 1986
Marfan syndrome: exclusion of genetic linkage to the COL1A2 geneP Tsipouras, A L Børresen, S Bamforth, et al.
Pageof 35