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Human genetics

Showing results (1121-1130 of 9,569) with videos related to

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Human Genetics|July 12, 1978
Evidence for subtypic determinants in the HLA-DW3 clusterD Niese, H Grosse-Wilde, B Dupont, et al.
Human Genetics|January 1, 1980
Inherited erythrocyte phosphofructokinase deficiency: molecular mechanismJ Etiemble, C Picat, J Siméon, et al.
Human Genetics|June 29, 1976
The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolismM Cantz, J Gehler
Human Genetics|January 1, 1984
Hyalinosis cutis et mucosae in siblingsE Haneke, O P Hornstein, M Meisel-Stosiek, et al.
Human Genetics|January 1, 1982
Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28)K B Nielsen, N Tommerup, H V Dyggve, et al.
Human Genetics|January 1, 1982
Isoelectric focusing of human red cell phosphoglucomutase (PGM1). Phenotype distribution in the population of Tuscany and two hereditary variantsM Bargagna, L Abbagnale
Human Genetics|January 1, 1984
Alpha-globin gene deletions associated with alpha A and alpha G Philadelphia in an Algerian family that includes two Hb G homozygotesF Morle, P Jaccoud, E Dorleac, et al.
Human Genetics|January 1, 1984
Bleomycin-induced chromosomal aberrations and sister chromatid exchanges in Down lymphocyte culturesK Iijima, K Morimoto, A Koizumi, et al.
Human Genetics|January 1, 1983
Variability in the phenotypic expression of abnormal sarcosine metabolism in a familyE S Kang, J Seyer, T A Todd, et al.
Human Genetics|January 1, 1984
The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19C Julier, D Weil, P Couillin, et al.
Pageof 957

Showing results (1121-1130 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|July 12, 1978
Evidence for subtypic determinants in the HLA-DW3 clusterD Niese, H Grosse-Wilde, B Dupont, et al.
Human Genetics|January 1, 1980
Inherited erythrocyte phosphofructokinase deficiency: molecular mechanismJ Etiemble, C Picat, J Siméon, et al.
Human Genetics|June 29, 1976
The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolismM Cantz, J Gehler
Human Genetics|January 1, 1984
Hyalinosis cutis et mucosae in siblingsE Haneke, O P Hornstein, M Meisel-Stosiek, et al.
Human Genetics|January 1, 1982
Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28)K B Nielsen, N Tommerup, H V Dyggve, et al.
Human Genetics|January 1, 1982
Isoelectric focusing of human red cell phosphoglucomutase (PGM1). Phenotype distribution in the population of Tuscany and two hereditary variantsM Bargagna, L Abbagnale
Human Genetics|January 1, 1984
Alpha-globin gene deletions associated with alpha A and alpha G Philadelphia in an Algerian family that includes two Hb G homozygotesF Morle, P Jaccoud, E Dorleac, et al.
Human Genetics|January 1, 1984
Bleomycin-induced chromosomal aberrations and sister chromatid exchanges in Down lymphocyte culturesK Iijima, K Morimoto, A Koizumi, et al.
Human Genetics|January 1, 1983
Variability in the phenotypic expression of abnormal sarcosine metabolism in a familyE S Kang, J Seyer, T A Todd, et al.
Human Genetics|January 1, 1984
The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19C Julier, D Weil, P Couillin, et al.
Pageof 957