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M Preus

Showing results (31-40 of 49) with videos related to

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Clinical Genetics|July 1, 1984
Trisomy 9 (pter----q1 to q3): the phenotype as an objective aid to karyotypic interpretationM Preus, A Schinzel, S Aymé, et al.
Journal De Genetique Humaine|December 1, 1983
An oculocerebral hypopigmentation syndromeM Preus, F C Fraser, F W Wiglesworth
Human Heredity|January 1, 1970
Dermatoglyphics in congenital heart malformationsM Preus, F C Fraser, E P Levy
American Journal of Medical Genetics|June 1, 1985
A taxonomic approach to the del(4p) phenotypeM Preus, S Aymé, P Kaplan, et al.
Birth Defects Original Article Series|January 1, 1975
The C syndromeM Preus, W J Alexander, F C Fraser
American Journal of Medical Genetics|July 1, 1983
Waardenburg syndrome--penetrance of major signsM Preus, C Linstrom, R C Polomeno, et al.
Journal of Ultrastructure Research|May 1, 1973
Homocellular and heterocellular gap junctions in Limulus: a thin-section and freeze-fracture studyR G Johnson, W S Herman, D M Preus
Toxicology Letters|August 1, 1988
Diagnostic value of serum creatine kinase and lactate dehydrogenase isoenzyme determinations for monitoring early cardiac damage in ratsM Preus, A S Bhargava, A E Khater, et al.
Arzneimittel-Forschung|March 1, 1990
Effect of iloprost on serum creatine kinase and lactate dehydrogenase isoenzymes after isoprenaline-induced cardiac damage in ratsA S Bhargava, M Preus, A R Khater, et al.
The Journal of Pediatrics|October 1, 1977
Familial occurrence of the Williams syndromeR A White, M Preus, G V Watters, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Clinical Genetics|July 1, 1984
Trisomy 9 (pter----q1 to q3): the phenotype as an objective aid to karyotypic interpretationM Preus, A Schinzel, S Aymé, et al.
Journal De Genetique Humaine|December 1, 1983
An oculocerebral hypopigmentation syndromeM Preus, F C Fraser, F W Wiglesworth
Human Heredity|January 1, 1970
Dermatoglyphics in congenital heart malformationsM Preus, F C Fraser, E P Levy
American Journal of Medical Genetics|June 1, 1985
A taxonomic approach to the del(4p) phenotypeM Preus, S Aymé, P Kaplan, et al.
Birth Defects Original Article Series|January 1, 1975
The C syndromeM Preus, W J Alexander, F C Fraser
American Journal of Medical Genetics|July 1, 1983
Waardenburg syndrome--penetrance of major signsM Preus, C Linstrom, R C Polomeno, et al.
Journal of Ultrastructure Research|May 1, 1973
Homocellular and heterocellular gap junctions in Limulus: a thin-section and freeze-fracture studyR G Johnson, W S Herman, D M Preus
Toxicology Letters|August 1, 1988
Diagnostic value of serum creatine kinase and lactate dehydrogenase isoenzyme determinations for monitoring early cardiac damage in ratsM Preus, A S Bhargava, A E Khater, et al.
Arzneimittel-Forschung|March 1, 1990
Effect of iloprost on serum creatine kinase and lactate dehydrogenase isoenzymes after isoprenaline-induced cardiac damage in ratsA S Bhargava, M Preus, A R Khater, et al.
The Journal of Pediatrics|October 1, 1977
Familial occurrence of the Williams syndromeR A White, M Preus, G V Watters, et al.
Pageof 5