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C Altay

Showing results (151-160 of 160) with videos related to

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Hemoglobin|January 1, 1986
Some notes about Hb Q-India and Hb Q-IranM Aksoy, A Gurgey, C Altay, et al.
Blood|May 1, 1989
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemiaJ M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.
American Journal of Hematology|December 1, 1993
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patientsM A Cürük, A J Dimovski, E Baysal, et al.
American Journal of Human Genetics|August 1, 1996
A locus for Fanconi anemia on 16q determined by homozygosity mappingM Gschwend, O Levran, L Kruglyak, et al.
Clinical Diabetes and Endocrinology|October 1, 2021
Risk factors for diabetic foot ulcers in metreleptin naïve patients with lipodystrophyO Saydam, B Ozgen Saydam, S C Adiyaman, et al.
American Journal of Human Genetics|April 17, 1999
The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significanceJ R Lo Ten Foe, M L Kwee, M A Rooimans, et al.
Blood|December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research GroupL Faivre, P Guardiola, C Lewis, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Heterogeneous spectrum of mutations in the Fanconi anaemia group A geneM Wijker, N V Morgan, S Herterich, et al.
Pageof 16

Showing results (151-160 of 160) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 160 results.
Hemoglobin|January 1, 1986
Some notes about Hb Q-India and Hb Q-IranM Aksoy, A Gurgey, C Altay, et al.
Blood|May 1, 1989
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemiaJ M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.
American Journal of Hematology|December 1, 1993
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patientsM A Cürük, A J Dimovski, E Baysal, et al.
American Journal of Human Genetics|August 1, 1996
A locus for Fanconi anemia on 16q determined by homozygosity mappingM Gschwend, O Levran, L Kruglyak, et al.
Clinical Diabetes and Endocrinology|October 1, 2021
Risk factors for diabetic foot ulcers in metreleptin naïve patients with lipodystrophyO Saydam, B Ozgen Saydam, S C Adiyaman, et al.
American Journal of Human Genetics|April 17, 1999
The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significanceJ R Lo Ten Foe, M L Kwee, M A Rooimans, et al.
Blood|December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research GroupL Faivre, P Guardiola, C Lewis, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Heterogeneous spectrum of mutations in the Fanconi anaemia group A geneM Wijker, N V Morgan, S Herterich, et al.
Pageof 16