1 was highly expressed upon both maternal and
paternal inheritance.
2 f AD is accounted for by excess maternal vs.
paternal inheritance,
a pattern consistent with mitochon
3 ectopic sites, with expression of Igf2 after
paternal inheritance and of H19 after maternal inheritan
4 This may present as larger increases on
paternal inheritance as in HD, or as a tendency to incre
5 After
paternal inheritance,
H19 was appropriately repressed an
6 for symbiont competition and recombination,
paternal inheritance has major consequences for expectat
7 e, the RNA-coding H19 gene is repressed upon
paternal inheritance in all species examined to date.
8 We did not observe
paternal inheritance in any of our patients.
9 To evaluate whether
paternal inheritance is a common phenomenon, we studied
10 In this family,
paternal inheritance leads to a normal phenotype, and ma
11 lethality, it was proposed that this reduced
paternal inheritance might be wholly or partially due to
12 Here we show that
paternal inheritance of a deletion of KvDMR1 results in
13 We find that
paternal inheritance of a deletion of the minimal Kcnq1o
14 Paternal inheritance of Ex1A-T leads to loss of imprinti
15 In adults,
paternal inheritance of Ex1A-T results in an increased m
16 Paternal inheritance of Ex1A-T-CON leads to loss of impr
17 In 2002,
paternal inheritance of muscle mitochondrial DNA (mtDNA)
18 Additionally, evidence of
paternal inheritance of plant mitochondria and recombina
19 ation before fertilization, thereby ensuring
paternal inheritance of the centrosome.
20 Paternal inheritance of the human PWS-IC demonstrates fo
21 Paternal inheritance of the mez1-m2 or mez1-m4 alleles c
22 ese phenotypes are seen on both maternal and
paternal inheritance of the mutant allele and are theref
23 While
paternal inheritance of the W. pipientis was not observe
24 Conversely,
paternal inheritance of these mutations disrupted mainte
25 On
paternal inheritance,
the (Ch beta GI)(2) was also hypom