Uniparental inheritance excludes organelles from sexual recombination.
Because the purpose of the submission is to obtain whole exome sequencing, inheritance excludes mitochondrial inheritance but includes autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive, Y-linked, isolated cases, and unknown inheritance.
In 1954, when the marquis died, the inheritance laws excluded illegitimate children.
Patients with chromosomal abnormalities, other multiorgan malformation syndromes, learning difficulties, known maternal exposure to significant teratogens during pregnancy, or family histories suggestive of Mendelian inheritance were excluded.
After inquiry of medical history, medical examination, and laboratory analysis, the possibilities of other diseases or diseases of genetic inheritance were excluded.
The sampling strategy for cosmogenic nuclides was designed to reduce the chance of nuclide inheritance, and exclude the possibility of nuclide loss through postglacial erosion.
This allows identification of regions of the genome that contain consecutive markers in which IBD inheritance is not excluded.
However other modes of inheritance cannot be excluded completely (e.g. genomic imprinting), but appear less likely.
The segregation analysis was consistent with an autosomal recessive inheritance; however, polygenic inheritance could not be excluded [ 87].
Consequently, as we excluded recessive inheritance to a great extent in the girl, an X-linked dominant mode of inheritance seems causative, either through a dominant-negative effect of the altered Naa10 protein in the NatA complex or a mixture of loss-of-function and dominant-negative effects.
