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Blood|December 26, 2008
Hematopoietic defects in the Ts1Cje mouse model of Down syndromeCatherine L Carmichael, Ian J Majewski, Warren S Alexander, et al.
Blood|October 1, 1985
Characterization of patients with an increased susceptibility to bacterial infections and a genetic deficiency of leukocyte membrane complement receptor type 3 and the related membrane antigen LFA-1G D Ross, R A Thompson, M J Walport, et al.
Gigascience|July 9, 2018
Clinker: visualizing fusion genes detected in RNA-seq dataBreon M Schmidt, Nadia M Davidson, Anthony D K Hawkins, et al.
Clinical Genetics|July 13, 2013
Whole-exome sequencing expands the phenotype of Hunter syndromeS M Nikkel, L Huang, R Lachman, et al.
Bioinformatics (Oxford, England)|July 17, 2012
A regression model for estimating DNA copy number applied to capture sequencing dataGuillem J Rigaill, Sidney Cadot, Roelof J C Kluin, et al.
Cancer Research|May 31, 2018
Integrative Modeling Identifies Key Determinants of Inhibitor Sensitivity in Breast Cancer Cell LinesKatarzyna Jastrzebski, Bram Thijssen, Roelof J C Kluin, et al.
Clinical Genetics|June 29, 2017
A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron lossT Paakkola, K Vuopala, H Kokkonen, et al.
Nucleic Acids Research|June 10, 2011
ChIP-seq analysis reveals distinct H3K27me3 profiles that correlate with transcriptional activityMatthew D Young, Tracy A Willson, Matthew J Wakefield, et al.
Polski Merkuriusz Lekarski : Organ Polskiego Towarzystwa Lekarskiego|November 18, 2000
[Quality of life in patients after implantation of pacemaker type DDD]J Lelakowski, P Podolec, J Majewski, et al.
Clinical Genetics|October 9, 2016
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactylyK D Kernohan, A McBride, Y Xi, et al.
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