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Hemoglobin
|
January 1, 1986
Some notes about Hb Q-India and Hb Q-Iran
M 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-thalassemia
J 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 patients
M 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 mapping
M 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 lipodystrophy
O 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 6p
Q 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/XRCC9
I 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 significance
J 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 Group
L 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 gene
M Wijker, N V Morgan, S Herterich, et al.
Page
of 16
Search research articles
Search
Showing results (151-160 of 160) with videos related to
Sort By:
Page
of 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-Iran
M 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-thalassemia
J 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 patients
M 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 mapping
M 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 lipodystrophy
O 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 6p
Q 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/XRCC9
I 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 significance
J 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 Group
L 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 gene
M Wijker, N V Morgan, S Herterich, et al.
Page
of 16