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J C Skare

Showing results (1-10 of 14) with videos related to

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The American Journal of the Medical Sciences|April 1, 1991
Presymptomatic and prenatal diagnosis of myotonic muscular dystrophy with linked DNA probesJ M Milunsky, J C Skare, A Milunsky
Human Genetics|July 1, 1989
Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on XqJ C Skare, J L Sullivan, A Milunsky
American Journal of Medical Genetics|September 1, 1991
Partial duplication of Xp: a case report and review of previously reported casesH E Wyandt, L Bugeau-Michaud, J C Skare, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1987
Mapping the X-linked lymphoproliferative syndromeJ C Skare, A Milunsky, K S Byron, et al.
American Journal of Obstetrics and Gynecology|March 1, 1991
Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probesA Milunsky, J C Skare, J M Milunsky, et al.
American Journal of Human Genetics|May 1, 1991
Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathyL A Jones, J C Skare, J A Harding, et al.
Clinical Genetics|January 1, 1991
A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90J C Skare, J M Milunsky, A Milunsky, et al.
Clinical Genetics|February 1, 1992
Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descentL A Jones, J C Skare, A S Cohen, et al.
American Journal of Medical Genetics|July 1, 1989
Chromosome deletion of Xq25 in an individual with X-linked lymphoproliferative diseaseH E Wyandt, H L Grierson, W G Sanger, et al.
American Journal of Human Genetics|September 1, 1989
Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAsJ C vanderSpek, H E Wyandt, J C Skare, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
The American Journal of the Medical Sciences|April 1, 1991
Presymptomatic and prenatal diagnosis of myotonic muscular dystrophy with linked DNA probesJ M Milunsky, J C Skare, A Milunsky
Human Genetics|July 1, 1989
Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on XqJ C Skare, J L Sullivan, A Milunsky
American Journal of Medical Genetics|September 1, 1991
Partial duplication of Xp: a case report and review of previously reported casesH E Wyandt, L Bugeau-Michaud, J C Skare, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1987
Mapping the X-linked lymphoproliferative syndromeJ C Skare, A Milunsky, K S Byron, et al.
American Journal of Obstetrics and Gynecology|March 1, 1991
Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probesA Milunsky, J C Skare, J M Milunsky, et al.
American Journal of Human Genetics|May 1, 1991
Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathyL A Jones, J C Skare, J A Harding, et al.
Clinical Genetics|January 1, 1991
A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90J C Skare, J M Milunsky, A Milunsky, et al.
Clinical Genetics|February 1, 1992
Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descentL A Jones, J C Skare, A S Cohen, et al.
American Journal of Medical Genetics|July 1, 1989
Chromosome deletion of Xq25 in an individual with X-linked lymphoproliferative diseaseH E Wyandt, H L Grierson, W G Sanger, et al.
American Journal of Human Genetics|September 1, 1989
Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAsJ C vanderSpek, H E Wyandt, J C Skare, et al.
Pageof 2