chromosomal crossover造句

• chromosomal crossover    In eukaryotes, recombination during meiosis is facilitated by chromosomal crossover. How common is chromosomal crossover in animal reproduction? Chromosomal crossover is when two DNA helic...
• chromosomal    The chromosomal material was obtained from cheek scrapings and hair roots. The genetic material is inspected for chromosomal damage and gene mutations. The rare chromosomal deficiency affe...
• chromosomal abberations    The R . A . El-Zein study says it will cause chromosomal abberations. :That study only tested lymphocytes for chromosomal abberations, so this would be called " need for further testing . ...
• chromosomal aberration    Chromosomal aberrations involving this gene are associated with endometrial stromal tumors. This approach can also be used to study chromosomal aberrations in fetal and neonatal genomes. A...
• chromosomal aberrations    Chromosomal aberrations involving this gene are associated with endometrial stromal tumors. This approach can also be used to study chromosomal aberrations in fetal and neonatal genomes. C...
• chromosomal abnormalities    The second chromosomal abnormality is called heterochromatin repulsion ( HR ). It's an chromosomal abnormality that only affects girls and women. Down syndrome is a chromosomal abnormality...
• chromosomal abnormality    Chromosomal abnormalities can lead to a delay in switching from embryonic hemoglobin. Genetic mutations and chromosomal abnormalities are two sources of HPG axis alteration. Some may be si...
• chromosomal analysis    Chromosomal analysis is necessary for definitive diagnosis. Since chromosomal analysis or karyotype testing is not a routine investigation for patients with epilepsy, the diagnosis of ring...
• chromosomal anomalies    Downs syndrome is a chromosomal anomaly. Such chromosomal anomalies as trisomy 13 and trisomy 18 have been found in association with holoprosencephaly, or other neural tube defects. Analys...
• chromosomal anomaly    Downs syndrome is a chromosomal anomaly. These birth defects included neural tube defects, malformations of the cardiac septa, anomalies of arteries and veins, and chromosomal anomalies. S...
• chromosomal arm    As usual in " Myotis " species, " Myotis alcathoe " has a karyotype consisting of 44 chromosomes, with the fundamental number of chromosomal arms equal to 52. According to some observation...
• chromosomal band    Moreover, various protocols and methods of analyzing IDPs, such as studies based on quantitative analysis of GC content in genes and their respective chromosomal bands, have been used to u...
• chromosomal break    Cells of Werner syndrome patients exhibit a reduced reproductive lifespan with chromosomal breaks and translocations, as well as large deletions of chromosomal components, causing genomic ...
• chromosomal breakage    Powerful mutagens may result in chromosomal instability, causing chromosomal breakages and rearrangement of the chromosomes such as inversion. The primary diagnostic test for Fanconi anaem...
• chromosomal breakage syndrome    Causes of partial insufficiencies of T cell function include acquired immune deficiency syndrome ( AIDS ), and hereditary conditions such as DiGeorge syndrome ( DGS ), chromosomal breakage...
• chromosomal change    This chromosomal change deletes the region of chromosome 15 that includes the UBE3A gene. This chromosomal change is associated with the development of AML following chemotherapy for other...
• chromosomal complement    In other cases, there are structural alterations ( chromosomal translocations, deletions . . . ) that modify the standard chromosomal complement. This uniqueness of the Y-chromosomal compl...
• chromosomal condition    1q21.1 microdeletion is a very rare chromosomal condition. Other tests revealed a rare chromosomal condition that could have led to severe retardation and death. The chromosomal conditions...
• chromosomal configuration    Although this process is not well understood, high-resolution imaging of live mouse oocytes has revealed that chromosomes form an intermediate chromosomal configuration, called the " prome...
• chromosomal defect    Genetic diseases may be divided into single-gene defects, multiple-gene disorders, or chromosomal defects. The problems included abnormalities of the heart, kidneys and urogential system, ...
• chromosomal defects    Genetic diseases may be divided into single-gene defects, multiple-gene disorders, or chromosomal defects. The problems included abnormalities of the heart, kidneys and urogential system, ...
• chromosomal deficiency    The rare chromosomal deficiency affects one in 2, 500 females. The chromosomal deficiency was discovered in 1959 . How do I know if I have Turner's syndrome? Railroad spokesman Richard Rus...
• chromosomal deletion    An amorphic allele elicits the same phenotype when chromosomal deletion or deficiency that disrupts the same gene. As the 18q chromosomal deletions were never resolved to be related solely...
• chromosomal deletion syndrome    Examples of chromosomal deletion syndromes include 4p-Deletion ( Wolf-Hirschhorn syndrome ), Prader Willi syndrome, and Angelman syndrome.
• chromosomal deletion syndromes    Examples of chromosomal deletion syndromes include 4p-Deletion ( Wolf-Hirschhorn syndrome ), Prader Willi syndrome, and Angelman syndrome.