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Jabs Ethylin Wang
Jabs E.W.
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http://hub.abes.fr/bmj/periodical/jmedgenet/2006/volume_43/issue_2/B3598D6B63057CBEE053120B220A90C5/authorship/8
http://hub.abes.fr/bmj/periodical/jmg/2009/volume_47/issue_1/B3598D6B65677CBEE053120B220A90C5/authorship/17
http://hub.abes.fr/bmj/periodical/jmedgenet/2006/volume_43/issue_7/B3598D6B63717CBEE053120B220A90C5/authorship/4
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_7/101093hmg471229/authorship/8
http://hub.abes.fr/bmj/periodical/jmg/2012/volume_49/issue_6/B35958AFB07E6AAFE053120B220A26C8/authorship/24
http://hub.abes.fr/bmj/periodical/jmedgenet/2006/volume_43/issue_2/B3598D6B63027CBEE053120B220A90C5/authorship/19
http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_14/101093hmgddn116/authorship/26
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_3/101093hmg13216a/authorship/4
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_7/101093hmgddi083/authorship/4
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_1/101093hmg61137/authorship/12
http://hub.abes.fr/springer/periodical/439/1994/volume_93/issue_5/B927DD9E85C25D90E053120B220A1EA8/authorship/1
http://hub.abes.fr/springer/periodical/11188/1984/volume_10/issue_1/B8F3FC40B94B0E61E053120B220A409A/authorship/1
http://hub.abes.fr/springer/periodical/335/1991/volume_1/issue_4/B8CA678C352366D6E053120B220A2E8F/authorship/6
http://hub.abes.fr/springer/periodical/412/1995/volume_104/issue_2/B90042FE3586304DE053120B220A9A23/authorship/3
http://hub.abes.fr/springer/periodical/412/1991/volume_100/issue_4/B90042FE2EE7304DE053120B220A9A23/authorship/1
http://hub.abes.fr/springer/periodical/439/1988/volume_78/issue_3/B9279D37F77F5861E053120B220A3025/authorship/4
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Characterization of reiterated human DNA with respect to mammalian X chromosome homology
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of FGFR2
Gene expression in pharyngeal arch 1 during human embryonic development
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity
Dinucleotide repeat polymorphism in the human fibroblast growth factor acidic (FGFA) gene on chromosome 5
Chromosomal localization of genes required for the terminal steps of oxidative metabolism: α and γ subunits of ATP synthase and the phosphate carrier
Studies of mitotic and centromeric abnormalities in Roberts syndrome: Implications for a defect in the mitotic mechanism
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene
Human gamma X satellite DNA: an X chromosome specific centromeric DNA sequence
Analysis of DNA restriction fragments greater than 5.7 Mb in size from the centromeric region of human chromosomes
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