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L Kalaydjieva

Showing results (1-10 of 70) with videos related to

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Journal of Medical Genetics|September 1, 1992
Screening for phenylketonuria in a totalitarian stateL Kalaydjieva, I Kremensky
American Journal of Clinical Pathology|September 1, 1989
Avoiding sources of error in PKU screeningI Kremensky, L Kalaydjieva
BMC Medical Genetics|April 12, 2001
Genetic studies of the Roma (Gypsies): a reviewL Kalaydjieva, D Gresham, F Calafell
Human Genetics|February 1, 1994
Detection of carriers of deletions in the dystrophin gene in Bulgarian DMD-BMD familiesJ Bronzova, A Todorova, L Kalaydjieva
Human Heredity|January 1, 1991
Further evidence of cystic fibrosis heterogeneity in southern EuropeL Kalaydjieva, P Plageras, J Horst
Journal of Medical Genetics|October 1, 1989
The molecular basis of beta thalassaemia in BulgariaL Kalaydjieva, A Eigel, J Horst
Human Molecular Genetics|January 1, 1994
Identification of six novel mutations in the CFTR gene of patients from Bulgaria by screening the twenty seven exons and exon/intron boundaries using DGGE and direct DNA sequencingA Savov, B Mercier, L Kalaydjieva, et al.
Human Genetics|October 1, 1991
A frameshift mutation in exon 2 of the phenylalanine hydroxylase gene linked to RFLP haplotype 1A Eigel, B Dworniczak, L Kalaydjieva, et al.
Human Genetics|September 1, 1990
Molecular data on cystic fibrosis in BulgariaL Kalaydjieva, J Antov, J Bronzova, et al.
Nucleic Acids Research|December 25, 1992
High percentage acrylamide gels improve resolution in SSCP analysisA Savov, D Angelicheva, A Jordanova, et al.
Pageof 7

Showing results (1-10 of 70) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|September 1, 1992
Screening for phenylketonuria in a totalitarian stateL Kalaydjieva, I Kremensky
American Journal of Clinical Pathology|September 1, 1989
Avoiding sources of error in PKU screeningI Kremensky, L Kalaydjieva
BMC Medical Genetics|April 12, 2001
Genetic studies of the Roma (Gypsies): a reviewL Kalaydjieva, D Gresham, F Calafell
Human Genetics|February 1, 1994
Detection of carriers of deletions in the dystrophin gene in Bulgarian DMD-BMD familiesJ Bronzova, A Todorova, L Kalaydjieva
Human Heredity|January 1, 1991
Further evidence of cystic fibrosis heterogeneity in southern EuropeL Kalaydjieva, P Plageras, J Horst
Journal of Medical Genetics|October 1, 1989
The molecular basis of beta thalassaemia in BulgariaL Kalaydjieva, A Eigel, J Horst
Human Molecular Genetics|January 1, 1994
Identification of six novel mutations in the CFTR gene of patients from Bulgaria by screening the twenty seven exons and exon/intron boundaries using DGGE and direct DNA sequencingA Savov, B Mercier, L Kalaydjieva, et al.
Human Genetics|October 1, 1991
A frameshift mutation in exon 2 of the phenylalanine hydroxylase gene linked to RFLP haplotype 1A Eigel, B Dworniczak, L Kalaydjieva, et al.
Human Genetics|September 1, 1990
Molecular data on cystic fibrosis in BulgariaL Kalaydjieva, J Antov, J Bronzova, et al.
Nucleic Acids Research|December 25, 1992
High percentage acrylamide gels improve resolution in SSCP analysisA Savov, D Angelicheva, A Jordanova, et al.
Pageof 7