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Craig I. W.
Craig Ian W.
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Craig I.W.
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http://hub.abes.fr/oup/periodical/nar/1992/volume_20/issue_3/101093nar203642/authorship/2
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_7/101093hmg371053/authorship/9
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_8/101093hmg681233/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_20/101093hmg9202993/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_8/101093hmgddp051/authorship/13
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_10/101093hmg2101727/authorship/6
http://hub.abes.fr/oup/periodical/hmg/2004/volume_13/issue_19/101093hmgddh239/authorship/18
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_3/101093hmg13161/authorship/8
http://hub.abes.fr/oup/periodical/nar/2005/volume_33/issue_3/101093nargni028/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_8/101093hmg18662/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_10/101093hmgddi142/authorship/6
http://hub.abes.fr/oup/periodical/nar/1992/volume_20/issue_6/101093nar2061429/authorship/4
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_4/101093hmg14286/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_5/101093hmg85915/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_2/101093hmg1283/authorship/8
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_3/101093hmg13187/authorship/5
http://hub.abes.fr/springer/periodical/10528/1976/volume_14/issue_1_2/B8ECC9ACD367549AE053120B220A6EB6/authorship/2
http://hub.abes.fr/springer/periodical/10528/1973/volume_9/issue_4/B8ECC9ACD035549AE053120B220A6EB6/authorship/1
http://hub.abes.fr/springer/periodical/439/1988/volume_80/issue_3/B927DD9E83845D90E053120B220A1EA8/authorship/6
http://hub.abes.fr/springer/periodical/439/1990/volume_84/issue_5/B927DD9E8C165D90E053120B220A1EA8/authorship/5
http://hub.abes.fr/springer/periodical/439/1989/volume_81/issue_3/B9279D37F74D5861E053120B220A3025/authorship/6
http://hub.abes.fr/springer/periodical/709/1971/volume_72/issue_2_3/B939E19FFF8D1544E053120B220A44EC/authorship/3
http://hub.abes.fr/springer/periodical/10528/1980/volume_18/issue_9_10/B8EC97DEF3974C62E053120B220A0C94/authorship/5
http://hub.abes.fr/springer/periodical/10545/1994/volume_17/issue_4/B8DD76546FCC2FF1E053120B220A8ECF/authorship/1
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_2/B8CA678C38BB66D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/439/1992/volume_88/issue_6/B927678D915B5706E053120B220AC130/authorship/5
http://hub.abes.fr/springer/periodical/10528/1975/volume_13/issue_11_12/B8ECC9ACD075549AE053120B220A6EB6/authorship/2
http://hub.abes.fr/springer/periodical/439/1992/volume_89/issue_2/B927678D92BC5706E053120B220AC130/authorship/6
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Organization of the human genome
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome
Dinucleotide repeat polymorphism at the human dopamine β-hydroxylase (DBH) locus
Characterization of a mutation within the NDP gene in a family with a manifesting female carrier
Characterisation of Renal Chloride Channel, CLCN5, Mutations in Hypercalciuric Nephrolithiasis (Kidney Stones) Disorders
Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder
SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene
Characterization of a YAC containing part or all of the Norrie disease locus
A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine β-hydroxylase locus
Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb
Dinucleotide repeat polymorphism in CEA gene
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia
DNA Pooling Identifies QTLs on Chromosome 4 for General Cognitive Ability in Children
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the Monoamine Oxidase A gene
Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships
Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp)
A procedure for the analysis of citrate synthase (E.C. 4.1.3.7) in somatic cell hybrids
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11
Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27β (DXS255)
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β
Assignment of a gene for tryptophanyl-transfer ribonucleic acid synthetase (E.C. 6.1.1.2) to human chromosome 14
Presence of two forms of fumarase (fumarate hydratase E.C. 4.2.1.2) in mammalian cells: Immunological characterization and genetic analysis in somatic cell hybrids. Confirmation of the assignment of a gene necessary for the enzyme expression to human chromosome 1
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.)
Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2
A comparison of the fine structure and nucleic acid biochemistry of chloroplasts and blue-green algae
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