Encyclopedia results for autosome

1. Autosome
   
   An autosome is a non sex chromosome . It is an ordinarily paired ref In the case of higher ploidy levels than the usual diploid, there will be the same number of an autosome as the ploidy level itself ..
   
   
   
   
2. Allosome
   
   An allosome is a sex chromosome that differs from an ordinary autosome in form, size, or behavior. The human sex chromosome s are a typical pair of allosomes. The x chromosomes are present in ovum, and the y ..
   
   
   
   
3. X:A ratio
   
   notability date January 2008 expert subject Genetics date May 2008 unreferenced date May 2008 The X A ratio is the ratio between the X chromosome and the number of sets of autosome s in an organism . ...
   
   
   
   
4. OmniPop
   
   Notability date April 2008 OmniPop is a program used to class populations by Autosome autosomal DNA results. It is a Microsoft Excel file & requires Excel to run. The program is recognized and used by National ..
   
   
   
   
5. Ecogenetics diseases
   
   influence as polygenic. Malignant lymphothermia An autosome autosomal dominant disease ..
   
   
   
   
6. Gigantiform cementoma
   
   Gigantiform cementoma is a rare, autosome autosomal tooth dental tumor . It is benign, but without intervention it can result in severe disfigurement of the jaw. The cause of this tumor is currently unknown ..
   
   
   
   
7. Klaus Patau
   
   anomaly caused by an extra autosome. The Lancet, 1960, I 790. ref . The syndrome caused by trisomy ..
   
   
   
   
8. Drosophila hybrid sterility
   
   has a role in hybrid male sterility. The possible interactions of Y chromosome are X Y, Y autosome ..., this would naturally result in fertility because of the Y dominant autosome interactions, therefore ..
   
   
   
   
9. Ohno's law
   
   species was located on an autosome in the other species. ref name ohno1967 Conservation mechanisms ... have not occurred due to its incompatibility with the sex determining mechanism. Moreover, X autosome ..
   
   
   
   
10. Atelosteogenesis, type II
    
    is an autosomal recessive disorder, which means the defective gene is located on an autosome , and two ..
    
    
    
    
11. Synapsis
    
    While autosome s undergo synapsis during meiosis sex chromosome s usually remain unpaired. ref cite ..
    
    
    
    
12. Behr's syndrome
    
    gene autosomal recessive , which means the defective gene is located on an autosome , and two copies ..
    
    
    
    
13. Impossible syndrome
    
    on an autosome , and two copies of the gene one from each parent are required to have an infant ..
    
    
    
    
14. Nager syndrome
    
    and lead productive lives. Inheritance pattern said to be Autosome autosomal but there are arguments ..
    
    
    
    
15. Galactose epimerase deficiency
    
    which means the defective gene is located on an autosome , and two copies of the defective gene one ..
    
    
    
    
16. Upington disease
    
    About orphan drugs Bot generated title ref This means the defective gene is located on an autosome ..
    
    
    
    
17. Beta-mannosidosis
    
    deficiency , ref OMIM 248510 ref is a rare autosome autosomal dominance genetics recessive ref name ..
    
    
    
    
18. Atransferrinemia
    
    , ref OMIM 209300 ref is an autosome autosomal dominance genetics recessive ref cite journal ... in an Autosome autosomal Recessive gene recessive pattern. ref cite journal language German pmid ..
    
    
    
    
19. EEM syndrome
    
    292 year 1989 pmid 2628819 doi 10.3109 13816818909009884 ref is an autosome autosomal recessive gene ... gene is located on an autosome, and two copies of the defective gene one from each parent are required ..
    
    
    
    
20. Ichthyosis lamellaris
    
    means the defective gene is located on an autosome , and both parents must carry one copy of the defective ..
    
    
    
    
21. Aase syndrome
    
    to be an autosome autosomal Dominant gene dominant inherited disorder. The genetic basis of the disease ..
    
    
    
    
22. Infantile neuronal ceroid lipfuscinosis
    
    ref is a form of Neuronal ceroid lipofuscinosis NCL and inherited as a recessive autosome autosomal ..
    
    
    
    
23. Carnitine palmitoyltransferase I deficiency
    
    has an autosomal recessive inheritance pattern, which means the defective gene is located on an autosome ..
    
    
    
    
24. Carnitine-acylcarnitine translocase deficiency
    
    , which means the defective gene is located on an autosome , and two copies of the gene one from ..
    
    
    
    
25. Hypochondrogenesis
    
    an autosomal dominant disorder because the affected gene is located on an autosome , and only one ..
    
    
    
    

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