Literature DB >> 8817350

Saturation multipoint linkage mapping of chromosome 6q in type 1 diabetes.

J L Davies1, F Cucca, J V Goy, Z A Atta, M E Merriman, A Wilson, A H Barnett, S C Bain, J A Todd.   

Abstract

Linkage analysis of type 1 diabetes sib pair families (n = 334) has suggested two separate regions of human chromosome 6q are linked to disease (designated IDDM5 and IDDM8). To test if these are false positive results, all available sib pair families (n = 429) were typed using a 92% informative map of chromosome 6q and multipoint analysis. The two regions still showed positive evidence of linkage, most notably the proterminal region, 6q27, corresponding to IDDM8 (MLS = 2.57, p = 0.0006; lambda s = 1.17). In addition, some evidence of transmission disequilibrium was seen with marker a046xa9 (IDDM5).

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Year:  1996        PMID: 8817350     DOI: 10.1093/hmg/5.7.1071

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  10 in total

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Authors:  H Zhao; K R Merikangas; K K Kidd
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5.  Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities.

Authors:  S Das; C M Lese; M Song; J L Jensen; L A Wells; B L Barnoski; J A Roseberry; J M Camacho; D H Ledbetter; R E Schnur
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  10 in total

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