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P S Harper

Showing results (71-80 of 345) with videos related to

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Annals of Neurology|September 1, 1991
Single-gene neurological disorders in South Wales: an epidemiological studyJ C MacMillan, P S Harper
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Presymptomatic testing for late-onset genetic disorders: lessons from Huntington's diseaseD M Ball, P S Harper
Journal of Medical Genetics|June 14, 2001
Prenatal testing for Huntington's disease: experience within the UK 1994-1998S A Simpson, P S Harper,
BMJ (Clinical Research Ed.)|February 18, 1989
Predictive testing for Huntington's diseaseP S Harper, M J Morris
British Medical Bulletin|July 1, 1989
Myotonic dystrophy: developments in molecular geneticsD J Shaw, P S Harper
Human Genetics|January 1, 1982
Incidence of Hunter's syndromeI D Young, P S Harper
Archives of Disease in Childhood|November 1, 1982
Mild form of Hunter's syndrome: clinical delineation based on 31 casesI D Young, P S Harper
Birth Defects Original Article Series|May 1, 1971
Kallmann syndromeR M Blizzard, P S Harper
Developmental Medicine and Child Neurology|August 1, 1983
The natural history of the severe form of Hunter's syndrome: a study based on 52 casesI D Young, P S Harper
Neurology|May 1, 1973
Congenital dystrophia myotonicaP R Dyken, P S Harper
Pageof 35

Showing results (71-80 of 345) with videos related to

Sort By:
Pageof 35
Annals of Neurology|September 1, 1991
Single-gene neurological disorders in South Wales: an epidemiological studyJ C MacMillan, P S Harper
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Presymptomatic testing for late-onset genetic disorders: lessons from Huntington's diseaseD M Ball, P S Harper
Journal of Medical Genetics|June 14, 2001
Prenatal testing for Huntington's disease: experience within the UK 1994-1998S A Simpson, P S Harper,
BMJ (Clinical Research Ed.)|February 18, 1989
Predictive testing for Huntington's diseaseP S Harper, M J Morris
British Medical Bulletin|July 1, 1989
Myotonic dystrophy: developments in molecular geneticsD J Shaw, P S Harper
Human Genetics|January 1, 1982
Incidence of Hunter's syndromeI D Young, P S Harper
Archives of Disease in Childhood|November 1, 1982
Mild form of Hunter's syndrome: clinical delineation based on 31 casesI D Young, P S Harper
Birth Defects Original Article Series|May 1, 1971
Kallmann syndromeR M Blizzard, P S Harper
Developmental Medicine and Child Neurology|August 1, 1983
The natural history of the severe form of Hunter's syndrome: a study based on 52 casesI D Young, P S Harper
Neurology|May 1, 1973
Congenital dystrophia myotonicaP R Dyken, P S Harper
Pageof 35