Searching journal content for articles similar to Shaheen et al. 24 (2): 291.

Displaying results 1-3 of 3
For checked items
  1. Research: Conservation of replication timing reveals global and local regulation of replication origin activity
    • Carolin A. Müller and
    • Conrad A. Nieduszynski
    Genome Res. October 2012 22: 1953-1962; Published in Advance July 5, 2012, doi:10.1101/gr.139477.112
    ...Conservation of replication timing reveals global and local regulation of replication origin activity Carolin A. Müller and Conrad A. Nieduszynski 1 Centre for Genetics and Genomics, The University of Nottingham, Medical School, Queen's Medical Centre...
    OPEN ACCESS ARTICLE
  2. Research: Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome
    • Gilad D. Evrony,
    • Dwight R. Cordero,
    • Jun Shen,
    • Jennifer N. Partlow,
    • Timothy W. Yu,
    • Rachel E. Rodin,
    • R. Sean Hill,
    • Michael E. Coulter,
    • Anh-Thu N. Lam,
    • Divya Jayaraman,
    • Dianne Gerrelli,
    • Diana G. Diaz,
    • Chloe Santos,
    • Victoria Morrison,
    • Antonella Galli,
    • Ulrich Tschulena,
    • Stefan Wiemann,
    • M. Jocelyne Martel,
    • Betty Spooner,
    • Steven C. Ryu,
    • Princess C. Elhosary,
    • Jillian M. Richardson,
    • Danielle Tierney,
    • Christopher A. Robinson,
    • Rajni Chibbar,
    • Dana Diudea,
    • Rebecca Folkerth,
    • Sheldon Wiebe,
    • A. James Barkovich,
    • Ganeshwaran H. Mochida,
    • James Irvine,
    • Edmond G. Lemire,
    • Patricia Blakley,
    • and Christopher A. Walsh
    Genome Res. August 2017 27: 1323-1335; Published in Advance June 19, 2017, doi:10.1101/gr.219899.116
    ...and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children’s Hospital, Boston, Massachusetts 02115, USA; 2Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA; 3Broad Institute of MIT and Harvard, Cambridge, Massachusetts...
    OPEN ACCESS ARTICLE
  3. Research: Whole-genome sequencing of Atacama skeleton shows novel mutations linked with dysplasia
    • Sanchita Bhattacharya,
    • Jian Li,
    • Alexandra Sockell,
    • Matthew J. Kan,
    • Felice A. Bava,
    • Shann-Ching Chen,
    • María C. Ávila-Arcos,
    • Xuhuai Ji,
    • Emery Smith,
    • Narges B. Asadi,
    • Ralph S. Lachman,
    • Hugo Y.K. Lam,
    • Carlos D. Bustamante,
    • Atul J. Butte,
    • and Garry P. Nolan
    Genome Res. April 2018 28: 423-431; Published in Advance March 22, 2018, doi:10.1101/gr.223693.117
    ...in microcephalic osteodysplastic primordial dwarfism type II (MOPDII), which is characterized by short bones and microcephaly. FLNB is important for fetal skeletal development and FLNB mutations are associated with atelosteogenesis I, Larsen syndrome, and spondylocarpotarsal synostosis syndrome, a disease...
    OPEN ACCESS ARTICLE
For checked items

Search Results

New Search

Modify Results

Citation format:
Results / page:
Results order:

This search

  • Alert me when new articles matching this search are published
  • Download all citations on this page to my citation manager

Preprint Server



Current Issue

  1. March 2026, 36 (3)
  1. Current Issue
  1. Alert me to new issues of Genome Research