Sentence examples for standard karyotypes from inspiring English sources

The highest African ancestry in the 187 consensus Standard karyotypes is 920 kb, whereas line 83 has African identity for 5840 kb.

B chromosomes are additional to standard karyotypes and may vary in size, number and morphology even between cells of the same individual.

These more common inversion types are substantially differentiated from the Standard karyotypes and cause LD (Corbett-Detig and Hartl 2012; Langley et al. 2012; Huang et al. 2014).

17 Because of the increased number of visible bands, small structural chromosomal abnormalities such as deletions or duplications not resolvable with standard karyotypes may be detected.

It is interesting that both Capreolus and Mazama genera likely possess identical standard karyotypes (2n = 70 + Bs) and have GC-rich small B chromosomes, which may suggest a common ancestry of supernumerary elements.

Otherwise indistinguishable from mice with the standard karyotype, some karyotypic races show some reproductive isolation as a consequence of the mis-pairing of chromosomal heterozygotes in hybrids and the production of aneuploid gametes or complete meiotic arrest (reviewed in Garagna et al., 2014).

Renal and cardiac ultrasounds were normal as was audition and standard karyotyping.

Intersexuality presents itself in numerous different forms, occurring both in individuals with a standard karyotype (the chromosomal make-up of the body's cells) of 46, XX (female) or 46, XY (male), as well as in those with more unusual karyotype combinations such as 47, XXY or 47, XYY.

These results imply that in some cases, deletions ≥10 Mb can be missed by standard karyotyping, although this method is expected to detect CNVs ≥5 to 10 Mb [11].

In another study, intended to note genetic differences between Oryx species, karyotypes of Oryx species and subspecies – namely O. gazella, O. b. beisa, O. b. callotis, O. dammah and O. leucoryx – were compared with the standard karyotype of Bos taurus.

In conclusion, using high-resolution array CGH, we were able to delineate two critical regions for 7q deletions in myeloid leukemias that were not detectable using standard karyotyping.