Results 211 to 220 of about 8,590 (232)

Heterosis and Heterozygosis in Pearl Millet Forage Production¹

Crop Science, 1968
Well‐established inbred lines of pearl millet, Pennisetum typhoides, were used to develop seed lots with 0, 50, 75, and 100% heterozygosity. Total annual forage yields (three or four cuttings per year) from drilled plots of these seed lots in lattice‐square experiments supplied the data considered.
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[Heterozygosis H63D in patients with steatohepatitis and chronic hepatitis C].

La Clinica terapeutica, 2007
Classic hereditary hemochromatosis is an autosomal recessive iron-overload disorder associated with mutation of the HFE gene. The homozygous genetic defect predisposes to a chain of events that may culminate in severe damage in multiple organs. Pathologic implications of heterozygous defect are still questionable; in fact since these individuals may ...
D, Pulvirenti, S, Neri, G, Bertino, N, Cutuli, L, Ignaccolo, M, Misseri, A, Tsami, L, Caruso   +7 more
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The amount of heterozygosis to be expected in an approximately pure line

Journal of Genetics, 1936
Heterozygosis in an approximately pure line is due to two causes. On the one hand, part of the heterozygosis of the original ancestors remains for some generations. Owing to linkage a few zygotes may have comparatively large heterozygous segments, but most of them are completely homozygous.
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The frequency oe heterozygosis in free-living populations ofdrosophila melanogaster anddrosophila subobsgura

Journal of Genetics, 1936
1. Free-living populations ofD. melanogaster andD. subobscura show a considerable incidence of heterozygosis for autosomal recessives. In 1933 frequencies wereD. subobscum 0.277 ±0.117,D. melanogaster 0.177±0.100, and in 1934D. subobscum 0.636 ± 0.149 andD. melanogaster 0.924 ± 0.251. Differences between successive years are largely accounted for by
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Unusual Presentation of Van Maldergem Syndrome in a Patient with DCHS1 Compound Heterozygosis. Further Expansion of the Phenotype?

Cytology and Genetics
Andrea D. Praticò
semanticscholar   +1 more source

[Biochemical and clinical studies of 2 new Italian cases of Hb G-Ferrara heterozygosis].

Bollettino della Societa italiana di biologia sperimentale, 1979
The Authors report the data concerning a family coming from Ficarolo (Rovigo). The father and one son were found hematologically healthy, but resulted carriers of Hb G-Ferrara. This is an unstable rare pigment with a replacement in the beta 57 (E-1) helicoidal position.
GUERRASIO, Angelo, SAGLIO, Giuseppe, CAMASCHELLA C., PICH PG, BARBERIS E., DEL PONTE D., IZZO P.   +6 more
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A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys)

Blood Coagulation and Fibrinolysis, 2016
A. Girolami, M. A. Molina, M. Galletti, S. Ferrari, L. Sambado, H. Guglielmone   +5 more
semanticscholar   +1 more source

Red Cell Exchange Transfusion in Severe HbS/Beta‐Thalassemia Double Heterozygosis

Vox Sanguinis, 1995
M. Gavoni, G.L. Lodi, M. Lunghi
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Heterozygote and Heterozygosis

2001
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Translocation heterozygosis in man.

American journal of human genetics, 1966
J M, Trujillo, R S, Zeller, R A, Plessala, B, List-Young   +3 more
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