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Severe Intrauterine Growth Retardation and Atypical Diabetes Associated with a Translocation Breakpoint Disrupting Regulation of the Insulin-Like Growth Factor 2 Gene

Murphy, R, Baptista, J, Holly, J, Umpleby, AM, Ellard, S, Harries, LW, Crolla, J, Cundy, T and Hattersley, AT (2008) Severe Intrauterine Growth Retardation and Atypical Diabetes Associated with a Translocation Breakpoint Disrupting Regulation of the Insulin-Like Growth Factor 2 Gene JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 93 (11). pp. 4373-4380.

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Item Type: Article
Authors :
NameEmailORCID
Murphy, RUNSPECIFIEDUNSPECIFIED
Baptista, JUNSPECIFIEDUNSPECIFIED
Holly, JUNSPECIFIEDUNSPECIFIED
Umpleby, AMUNSPECIFIEDUNSPECIFIED
Ellard, SUNSPECIFIEDUNSPECIFIED
Harries, LWUNSPECIFIEDUNSPECIFIED
Crolla, JUNSPECIFIEDUNSPECIFIED
Cundy, TUNSPECIFIEDUNSPECIFIED
Hattersley, ATUNSPECIFIEDUNSPECIFIED
Date : 1 November 2008
Identification Number : https://doi.org/10.1210/jc.2008-0819
Uncontrolled Keywords : Science & Technology, Life Sciences & Biomedicine, Endocrinology & Metabolism, ENDOCRINOLOGY & METABOLISM, ACID-LABILE SUBUNIT, FACTOR-II GENE, BECKWITH-WIEDEMANN-SYNDROME, SILVER-RUSSELL-SYNDROME, IGF2 GENE, CHROMOSOME 11P15, STAT5B MUTATION, DEFICIENCY, OBESITY, PHENOTYPE
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 09:14
Last Modified : 17 May 2017 09:14
URI: http://epubs.surrey.ac.uk/id/eprint/822871

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