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http://hub.abes.fr/bmj/periodical/jcp/2010/volume_63/issue_7/B3590AD5D5A27A9EE053120B220A165E/authorship/6
http://hub.abes.fr/bmj/periodical/jclinpath/2007/volume_60/issue_4/B3590AD5D1FD7A9EE053120B220A165E/authorship/4
http://hub.abes.fr/bmj/periodical/jclinpath/2007/volume_60/issue_1/B3590AD5D1537A9EE053120B220A165E/authorship/4
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_22/101093hmgddp379/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_26/101093hmg10262989/authorship/14
http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_10/101093hmgddn024/authorship/10
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_11/101093hmgddp117/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_10/101093hmg3101819/authorship/3
http://hub.abes.fr/oup/periodical/humrep/1993/volume_8/issue_3/101093oxfordjournalshumrepa138060/authorship/2
http://hub.abes.fr/oup/periodical/humrep/2000/volume_15/issue_11/101093humrep15112404/authorship/6
http://hub.abes.fr/oup/periodical/hmg/2006/volume_15/issue_6/101093hmgddl002/authorship/11
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_suppl1/101093hmgddg067/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_11/101093hmg11111317/authorship/16
http://hub.abes.fr/springer/periodical/335/1995/volume_6/issue_4/B8CA678C36FF66D6E053120B220A2E8F/authorship/2
http://hub.abes.fr/springer/periodical/439/1982/volume_61/issue_3/B9279D37F6E95861E053120B220A3025/authorship/1
http://hub.abes.fr/springer/periodical/439/1984/volume_66/issue_1/B9279D37F0915861E053120B220A3025/authorship/1
http://hub.abes.fr/springer/periodical/439/1985/volume_70/issue_4/B9279D37F4FA5861E053120B220A3025/authorship/1
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Characterization of abnormal one pronuclear human oocytes by morphology, cytogenetics and in-situ hybridization
A heat shock gene at 14q22: mapping and expression
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1
Identification of interactive networks of gene expression associated with osteosarcoma oncogenesis by integrated molecular profiling
Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma
Spontaneous blastomere fusion after freezing and thawing of early human embryos leads to polyploidy and chromosomal mosaicism
A role for Brca1 in chromosome end maintenance
The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region
Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome
Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development
A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma
Prenatal diagnosis and outcome of pregnancy in 2036 women investigated by amniocentesis
Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: Verification by standard staining techniques, new densitometric methods, and somatic cell hybridization
Mapping of the gonadotropin-releasing hormone (GnRH) receptor gene to human Chromosome 4q21.2 by fluorescence in situ hybridization
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