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M Telatar

Showing results (21-30 of 35) with videos related to

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The Turkish Journal of Pediatrics|April 1, 1992
Carrier detection by DNA analysis in Duchenne muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
Neurology|October 27, 1997
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxiaD H Geschwind, S Perlman, W W Grody, et al.
Journal of Endocrinological Investigation|July 6, 2004
Sphenoid sinus brown tumor, a mass lesion of occipital bone and hypercalcemia: an unusual presentation of primary hyperparathyroidismC Erem, A Hacihasanoglu, A Cinel, et al.
British Journal of Cancer|September 2, 1999
Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancerD G Bebb, Z Yu, J Chen, et al.
Clinical Lymphoma|November 15, 2001
Excellent tolerance of rituximab when given after mitoxantrone/cyclophosphamide: an effective and safe combination for indolent non-Hodgkin's lymphomaC Emmanouilides, P Rosen, M Telatar, et al.
Molecular Genetics and Metabolism|July 31, 1998
A model for ATM heterozygote identification in a large population: four founder-effect ATM mutations identify most of Costa Rican patients with ataxia telangiectasiaM Telatar, S Wang, S Castellvi-Bel, et al.
Human Mutation|January 1, 1994
Cystic fibrosis patients from the Black Sea region: the 1677delTA mutationD Angelicheva, K Boteva, A Jordanova, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effectK Laake, M Telatar, G A Geitvik, et al.
Human Mutation|July 29, 1999
New mutations, polymorphisms, and rare variants in the ATM gene detected by a novel SSCP strategyS Castellví-Bel, S Sheikhavandi, M Telatar, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Ataxia-telangiectasia: linkage analysis of chromosome 11q22-23 markers in Turkish familiesO Sanal, E Lange, M Telatar, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
The Turkish Journal of Pediatrics|April 1, 1992
Carrier detection by DNA analysis in Duchenne muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
Neurology|October 27, 1997
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxiaD H Geschwind, S Perlman, W W Grody, et al.
Journal of Endocrinological Investigation|July 6, 2004
Sphenoid sinus brown tumor, a mass lesion of occipital bone and hypercalcemia: an unusual presentation of primary hyperparathyroidismC Erem, A Hacihasanoglu, A Cinel, et al.
British Journal of Cancer|September 2, 1999
Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancerD G Bebb, Z Yu, J Chen, et al.
Clinical Lymphoma|November 15, 2001
Excellent tolerance of rituximab when given after mitoxantrone/cyclophosphamide: an effective and safe combination for indolent non-Hodgkin's lymphomaC Emmanouilides, P Rosen, M Telatar, et al.
Molecular Genetics and Metabolism|July 31, 1998
A model for ATM heterozygote identification in a large population: four founder-effect ATM mutations identify most of Costa Rican patients with ataxia telangiectasiaM Telatar, S Wang, S Castellvi-Bel, et al.
Human Mutation|January 1, 1994
Cystic fibrosis patients from the Black Sea region: the 1677delTA mutationD Angelicheva, K Boteva, A Jordanova, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effectK Laake, M Telatar, G A Geitvik, et al.
Human Mutation|July 29, 1999
New mutations, polymorphisms, and rare variants in the ATM gene detected by a novel SSCP strategyS Castellví-Bel, S Sheikhavandi, M Telatar, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Ataxia-telangiectasia: linkage analysis of chromosome 11q22-23 markers in Turkish familiesO Sanal, E Lange, M Telatar, et al.
Pageof 4