Results 341 to 350 of about 2,771,911 (398)
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Seminars in Pediatric Surgery, 2010
For many years karyotyping has been a successful tool to identify chromosome aberrations in congenital malformations. It has proven to be a highly reliable technique for identifying numerical chromosome changes and structural chromosomal rearrangements, such as deletions, duplications, translocations, or inversions.
de Klein, Annelies, Tibboel, Dick
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For many years karyotyping has been a successful tool to identify chromosome aberrations in congenital malformations. It has proven to be a highly reliable technique for identifying numerical chromosome changes and structural chromosomal rearrangements, such as deletions, duplications, translocations, or inversions.
de Klein, Annelies, Tibboel, Dick
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Introduction to Quantitative Genetics
Quantitative Genetics, 2012So far in this course we have dealt entirely either with the evolution of characters that are controlled by simple Mendelian inheritance at a single locus or with the evolution of molecular sequences.
G. Acquaah
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Molecular Evolutionary Genetics
, 1987Recent developments of statistical methods in molecular phylogenetics are reviewed. It is shown that the mathematical foundations of these methods are not well established, but computer simulations and empirical data indicate that currently used methods ...
M. Nei
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Calcified Tissue International, 1994
Osteoporosis (OP) is the most prevalent metabolic bone disease among developed countries and it is defined as a systemic skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue with a consequent increase in bone fragility and susceptibility to nontraumatic fracture [1].
BRANDI, MARIA LUISA +7 more
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Osteoporosis (OP) is the most prevalent metabolic bone disease among developed countries and it is defined as a systemic skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue with a consequent increase in bone fragility and susceptibility to nontraumatic fracture [1].
BRANDI, MARIA LUISA +7 more
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Principles of population genetics
, 1981Genetic and Phenotypic Variation Organisation of Genetic Variation Random Genetic Drift Mutation and the Neutral Theory Darwinian Selection Inbreeding, Population Subdivision, and Migration Molecular Population Genetics Evolutionary Quantitative Genetics
D. Hartl, A. Clark
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An introduction to population genetics theory
, 1971An introduction to population genetics theory , An introduction to population genetics theory , مرکز فناوری اطلاعات و اطلاع رسانی ...
J. Crow, M. Kimura
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Genetics and the Origin of the Genetic Code
Origins of Life, 1974The genetic code has been analysed by a method similar to that used by Gregor Mendel. The current codon catalogue is shown to be symmetrically subdivisible into two discrete subcatalogues of eight quartets each by classifying the quartets as monocoding (for one amino acid only) vs heterocoding (for two amino acids or for amino acid plus nonsense).
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Genetics and genetic testing for glaucoma
Current Opinion in Ophthalmology, 2017In recent decades, investigators have identified numerous genes and genetic factors that cause or contribute risk for glaucoma. These findings have increased our understanding of disease mechanisms, provided us with new diagnostic tools, and may allow for development of improved therapies for glaucoma. However, genetic testing is most useful when it is
Matthew A. Miller +2 more
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Genetic algorithms for genetic mapping [PDF]
, 1998 Constructing genetic maps is a prerequisite for most in-depth genetic studies of an organism. The problem of constructing reliable genetic maps for any organism can be considered as a complex optimization problem with both discrete and continuous parameters. This paper shows how genetic algorithms can been used to tackle this problem on simple pedigree.
Gaspin, Christine, Schiex, Thomas
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[Genetics and genetic counseling].
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2016Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most frequent genetic disease, characterized by progressive development of bilateral renal cysts. Two causative genes have been identified: PKD1 and PKD2. ADPKD phenotype is highly variable. Typically, ADPKD is an adult onset disease.
Izzi, Claudia +6 more
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