<\/p>\n
+ So, the parthenogenetic greenfly offspring are not identical, and do show some genetic variation: some chromosome<\/strong> segments differ because of meiosis.\n<\/p>\n <\/p>\n + Those that do use the sex chromosome<\/strong> system have variations in how it happens.\n<\/p>\n <\/p>\n + The mother’s Egg eggs always contain an X chromosome<\/strong><\/strong><\/strong>, while the father’s sperm contains either a Y chromosome<\/strong><\/strong><\/strong> or an X chromosome<\/strong><\/strong><\/strong>.\n<\/p>\n <\/p>\n + There are a few chromosome<\/strong> problems that babies can sometimes be born with.\n<\/p>\n <\/p>\n + Without it, the algae at the surface would suffer chromosome<\/strong> breaks and DNA mutations.\n<\/p>\n <\/p>\n + In 2008, a consensus definition of the epigenetic trait, “stably heritable phenotype resulting from changes in a chromosome<\/strong> without alterations in the DNA sequence”, was made at a Cold Spring Harbor meeting.\n<\/p>\n + The order of the genes on the chromosome<\/strong> is the same as the expression of the genes in the developing embryo.\n<\/p>\n <\/p>\n + DiGeorge syndrome is due to the deletion of 30 to 40 genes in the middle of chromosome<\/strong> 22 at a location known as “22q11.2”.\n<\/p>\n <\/p>\n + In the 1990s, genomegenomic studies of the world’s peoples found that the Y chromosome<\/strong> of San men share patterns of polymorphisms that are different from those of all other populations.\n<\/p>\n <\/p>\n + So, “as long as all the female queen mates only with one male”, all the female offspring will inherit the male’s chromosome<\/strong> 100% intact.\n<\/p>\n <\/p>\n + Their splitting into two equal longitudinal halves assured each daughter cell got the same chromosome<\/strong> complement.\n<\/p>\n <\/p>\n + When a part of a chromosome<\/strong> gets reversed end to end, so the genes run in the opposite direction to before.\n<\/p>\n <\/p>\n + It is used to indicate the number of chromosome<\/strong> sets in a cell.\n<\/p>\n <\/p>\n + The condition is autosomal dominant: only one affected chromosome<\/strong> is needed for the condition to occur.\n<\/p>\n <\/p>\n + Furthermore, the sequence of these control genes show “co-linearity”: the order of the Locus loci in the chromosome<\/strong> parallels the order in which the loci are expressed along the anterior-posterior axis of the body.\n<\/p>\n <\/p>\n + If they are, that chromosome<\/strong><\/strong> is called a sex chromosome<\/strong><\/strong>, and the genes on it are called ‘sex linked’.\n<\/p>\n <\/p>\n + The higher the percentage of offspring showing both traits, the closer on the chromosome<\/strong> the two genes are.\n<\/p>\n <\/p>\n + According to recent genetic analysis, both mtDNA and Y chromosome<\/strong> exist in Austrians.\n<\/p>\n <\/p>\n + Therefore, “the sperms are not identical”, because in each chromosome<\/strong> of a pair there will be different alleles at many of the loci.\n<\/p>\n <\/p>\n + A human fetus starts as female so the Y chromosome<\/strong> is what makes the changes necessary to switch to male.\n<\/p>\n <\/p>\n + Chromosome<\/strong> 21 was the second human chromosome<\/strong> to be completely sequenced.\n<\/p>\n <\/p>\n + The M subunit is coded by LDHA on human chromosome<\/strong><\/strong> 11, and the H subunit is coded by LDHB on chromosome<\/strong><\/strong> 12.\n<\/p>\n <\/p>\n + Infield crickets, for example, insects with a single X chromosome<\/strong> develop as male, while those with two develop as female.\n<\/p>\n <\/p>\n + At about the same time as Walther Flemming, and Edouard van Beneden, he worked out chromosome<\/strong> movement during mitosis in plant cells.\n<\/p>\n <\/p>\n + According to the study, more than half of the Y chromosome<\/strong> lineages that are seen in today’s Maltese population could have come in with the Phoenicians.\n<\/p>\n <\/p>\n + Other notable ecological geneticists would include Theodosius Dobzhansky who worked on chromosome<\/strong> polymorphism in fruit flies.\n<\/p>\n <\/p>\n + It was the first one given for genetics, for his “discoveries concerning the role played by the chromosome<\/strong> in heredity”.\n<\/p>\n <\/p>\n + He argued that chromosome<\/strong> number may be a useful tool for the construction of phylogenies.\n<\/p>\n <\/p>\n + The Y chromosome<\/strong><\/strong> does carry some genes, but far fewer than the X chromosome<\/strong><\/strong>.\n<\/p>\n <\/p>\n + Like most other male mammals, a man inherits an X chromosome<\/strong><\/strong> from his mother and a Y chromosome<\/strong><\/strong> from his father.\n<\/p>\n <\/p>\n + The function of telomeres is to avoid the loss of important DNA from chromosome<\/strong> ends.\n<\/p>\n <\/p>\n + The Q1* Y chromosome<\/strong> sublineage of Q-M242 is widespread among Asians and Native Americans and is thought to have originated in the Altai Mountains.\n<\/p>\n <\/p>\n + Every time the chromosome<\/strong> is copied 100\u2013200 meaningless nucleotides are lost, which causes no damage to the organism’s DNA.\n<\/p>\n <\/p>\n + A mutation on chromosome<\/strong> 2 stops the shutdown in lactase production.\n<\/p>\n <\/p>\n + Each chromosome<\/strong> contains many genes.\n<\/p>\n <\/p>\n + Another type of genetic defect is caused by errors in chromosome<\/strong> copying during the cell division which produces the gametes.\n<\/p>\n <\/p>\n + Anyone with three copies of chromosome<\/strong> 21 has Down syndrome, also known as trisomy 21.\n<\/p>\n <\/p>\n + In May 2000, researchers working on the Human Genome Project announced that the sequence of base pairs which make up this chromosome<\/strong> had been identified.\n<\/p>\n <\/p>\n + People with Down syndrome have an extra copy of chromosome<\/strong> 21, or part of it.\n<\/p>\n <\/p>\n + This happens when a normal chromosome<\/strong> breaks into two pieces.\n<\/p>\n <\/p>\n + Although females have two X chromosome<\/strong><\/strong>s, each cell can only have one X chromosome<\/strong><\/strong> active.\n<\/p>\n <\/p>\n + For example, Down syndrome happens when there are three copies of chromosome<\/strong> #21.\n<\/p>\n <\/p>\n + They sit next to each other on chromosome<\/strong> 15., “Journal of Human Genetics” 2011.\n<\/p>\n <\/p>\n + Histone modifications act in diverse biological processes such as gene regulation, DNA repair and chromosome<\/strong> condensation.\n<\/p>\n <\/p>\n + However, a female cat has two X chromosome<\/strong><\/strong>s, so it can have both versions, black on one chromosome<\/strong><\/strong> and orange on the other, making the cat a calico.\n<\/p>\n <\/p>\n + The human genome is stored on 23 chromosome<\/strong> pairs in the cell nucleus and in the small mitochondrial DNA.\n<\/p>\n <\/p>\n + Its main functions are to maintain a cell’s shape, cell motility, chromosome<\/strong> movement in cell division, and organelle movement.\n<\/p>\n <\/p>\n + Insights into the dynamics of genome size and chromosome<\/strong> evolution in the early diverging angiosperm lineage Nymphaeales.\n<\/p>\n <\/p>\n + The family is divided into four genusgenera based on their diploid chromosome<\/strong> number: “Hylobates”.\n<\/p>\n <\/p>\n + Studies over many years have shown that natural populations of “Drosophila” are polymorphic for chromosome<\/strong> inversions.\n<\/p>\n <\/p>\n + Prokaryotic cells such as bacterial cells reproduce by binary fission, a process that includes DNA replication, chromosome<\/strong> segregation, and cytokinesis.\n<\/p>\n <\/p>\n + Already, from the cells recovered by amniotic contuses, chromosome<\/strong> defects like triple-21 can be seen under the microscope.\n<\/p>\n <\/p>\n + A male cat usually has one X chromosome<\/strong><\/strong> and one Y chromosome<\/strong><\/strong>.\n<\/p>\n <\/p>\n + Crossing over is the exchange of chromosome<\/strong> segments between non-sister chromatids during the production of gametes.\n<\/p>\n <\/p>\n + So, alleles on the same chromosome<\/strong> can be separated and go to different daughter cells.\n<\/p>\n <\/p>\n + This mutation followed a previous mutation, which created the haplogroup known as haplogroup J-P209 or simply haplogroup J, and so this makes this Y chromosome<\/strong><\/strong> the “child” of the older version of the Y chromosome<\/strong><\/strong>.\n<\/p>\n <\/p>\n + There are two copies of chromosome<\/strong> 21 in most people.\n<\/p>\n <\/p>\n + DiGeorge syndrome, or 22q11.2 deletion syndrome, is a syndrome caused by the deletion deletion of a small segment of chromosome<\/strong> 22.\n<\/p>\n <\/p>\n + The genome is a circular chromosome<\/strong> of 159,662 base pairs and has a high coding density with many overlapping genes and reduced gene length.\n<\/p>\n <\/p>\n + All animals in this genus were part of the same species before, “Calomyscus bailwardi”, but they are now separate species because they have big differences in chromosome<\/strong> number, skull length and weight, and other differences.\n<\/p>\n <\/p>\n + An inversion is a chromosome<\/strong> rearrangement out of mutation.\n<\/p>\n <\/p>\n + Most embryos and fetuses with chromosome<\/strong> problems will not live for a long time.\n<\/p>\n <\/p>\n + The X chromosome<\/strong><\/strong> is one of the two sex chromosome<\/strong><\/strong>s in mammals.\n<\/p>\n <\/p>\n + These are regions of the chromosome<\/strong> that are important in preserving genetic information.\n<\/p>\n <\/p>\n + Sometimes even when the parent cells are normal chromosome<\/strong> 21 can be deformed when cells reproduce.\n<\/p>\n <\/p>\n![\"Sentence](\"https:\/\/englishteststore.net\/blog\/wp-content\/uploads\/2021\/09\/Sentence-example-of-chromosome.jpg\" "\\"Sentence")
Example sentences of “chromosome”:<\/h2>\n
+ The order of the genes on the chromosome<\/strong> is the same as the expression of the genes in the developing embryo.\r\n
+ DiGeorge syndrome is due to the deletion of 30 to 40 genes in the middle of chromosome<\/strong> 22 at a location known as \"22q11.2\".\r\n
+ In the 1990s, genomegenomic studies of the world's peoples found that the Y chromosome<\/strong> of San men share patterns of polymorphisms that are different from those of all other populations.\r\n
<\/pre>\nMore in-sentence examples of “chromosome”:<\/h2>\n