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lehrach h
(715 results)?
Transcriptome and genome sequencing uncovers functional variation in humans.
Nature. 2013 Sep 26;501(7468):506-11. doi: 10.1038/nature12531. Epub 2013 Sep 15.
Nature. 2013.
PMID: 24037378
Free PMC article.
Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing.
Ferreira PG, Oti M, Barann M, Wieland T, Ezquina S, Friedländer MR, Rivas MA, Esteve-Codina A; GEUVADIS Consortium; Rosenstiel P, Strom TM, Lappalainen T, Guigó R, Sammeth M.
Ferreira PG, et al.
Sci Rep. 2016 Sep 12;6:32406. doi: 10.1038/srep32406.
Sci Rep. 2016.
PMID: 27617755
Free PMC article.
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The (6;9) chromosome translocation, associated with a specific subtype of acute nonlymphocytic leukemia, leads to aberrant transcription of a target gene on 9q34.
von Lindern M, Poustka A, Lerach H, Grosveld G.
von Lindern M, et al. Among authors: lerach h.
Mol Cell Biol. 1990 Aug;10(8):4016-26. doi: 10.1128/mcb.10.8.4016-4026.1990.
Mol Cell Biol. 1990.
PMID: 2370860
Free PMC article.
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Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning.
Bergen AA, Wapenaar MC, Schuurman EJ, Diergaarde PJ, Lerach H, Monaco AP, Bakker E, Bleeker-Wagemakers EM, van Ommen GJ.
Bergen AA, et al. Among authors: lerach h.
Cytogenet Cell Genet. 1993;62(4):231-5. doi: 10.1159/000133484.
Cytogenet Cell Genet. 1993.
PMID: 8440142
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