Results 241 to 250 of about 82,434 (287)
Quantitative genetics of microbiome-mediated traits. [PDF]
Week B +4 more
europepmc +1 more source
The polyploid continuum and the landscape of polyploid genomic variation. [PDF]
Twyford AD +6 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Patterns of Genetic Inheritance
Neonatal Network, 1999Neonatal nurses need to understand the basic patterns of genetic transmission. This article, the first in a series, provides an overview of Mendel’s laws and discusses five types of transmission: single gene inheritance, chromosomal inheritance, multifactorial inheritance, cytoplasmic inheritance, and somatic cell mutations.
B A, Reyna, R H, Pickler
openaire +2 more sources
Atypical Patterns of Inheritance
Seminars in Pediatric Neurology, 2007The incomplete prediction of clinical phenotype from genotype in monogenic disorders assumes other complex mechanisms are responsible. Recent examples derived from well-known human diseases will be discussed in this review in the context of the roles of modifier genes, digenic and triallelic inheritance, and the consequence of imprinting and opposite ...
Andrea L, Gropman, David R, Adams
openaire +2 more sources
Patterns of alcoholism inheritance
Journal of Substance Abuse, 1992Like many other common, complex disorders, alcoholism tends to run in families. Evidence from animal studies as well as biochemical, electrophysiologic, and personality studies of alcoholics and their offspring indicate the existence of heritable factors predisposing to the development of alcoholism. Twin and adoption studies also support the idea that
openaire +2 more sources
Postgraduate Medicine, 1972
The first approach to analysis of the inheritance pattern of mendelian diseases depends on whether the mutant gene or genes are located on one of the 44 (22 pairs) autosomes or on the one or two X chromosomes. No human disease is known to be associated with a mutant gene on the Y chromosome.
openaire +2 more sources
The first approach to analysis of the inheritance pattern of mendelian diseases depends on whether the mutant gene or genes are located on one of the 44 (22 pairs) autosomes or on the one or two X chromosomes. No human disease is known to be associated with a mutant gene on the Y chromosome.
openaire +2 more sources

