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The identification of two cases of primary myelofibrosis which lack committed erythroid progenitor cells and which show in common a chromosomal defect on chromosome 11 point to the existence of genes on this chromosome which play a key role during erythropoiesis.
UPD, including UPD9p, appears to be a common chromosomal defect, occurring on chromosomes other than 9 in 8/30 patients (i.e. on chromosomes 1, 11, and 22) (Table 3).
i(17q) is the most common chromosomal defect in medulloblastoma, affecting 30 40% of cases, and chromosome 6 loss is characteristic of the molecular disease sub-group defined by activation of the Wnt/Wingless cell signalling pathway [1] [5].
I told her I had seen a guest on a talk show who was a male to female transsexual due to a chromosomal defect and asked if she would run a test on my chromosomes.
She and others also studied a lethal chromosomal defect that disrupts the normal function of the mouse liver.
If not, three bright oranges (trisomy) might appear, or one green (monosomy), suggesting a particular chromosomal defect.
Similar(33)
Chromosomal defects such as chromosome amplifications and deletions can be detected from the analysis of gene expression data [ 22, 23].
Chromosomal defects were referenced.
Different types of mitotic chromosomal defects in nuclear transfer embryos.
In women older than 37, who have a higher incidence of embryos with chromosomal defects, three to five embryos are still recommended, depending on the woman's age.
Doctors have long recommended an amniocentesis test for pregnant women 35 and over, whose age puts them at greater risk for chromosomal defects.
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