Literature DB >> 10777365

The continuing failure to recognise Alström syndrome and further evidence of genetic homogeneity.

V J Deeble, E Roberts, A Jackson, N Lench, G Karbani, C G Woods.   

Abstract

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Year:  2000        PMID： 10777365      PMCID： PMC1734548          DOI： 10.1136/jmg.37.3.219

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents.

Authors:  Klaas J Wierenga; Zhijie Jiang; Amy C Yang; John J Mulvihill; Nicholas F Tsinoremas
Journal:  Genet Med       Date:  2012-10-25       Impact factor: 8.822

2.  Alstrom syndrome in four sibs from northern Jordan.

Authors:  Hanan Hamamy; Muries Barham; Abd-ElKarim Alkhawaldeh; David Cockburn; Helen Snowden; Kamel Ajlouni
Journal:  Ann Saudi Med       Date:  2006 Nov-Dec       Impact factor: 1.526

3.  Alström syndrome: A rare association of retinitis pigmentosa with insulin resistance syndrome.

Authors:  Irfan Yousuf Wani; Ashraf Ganie; Iqra Mehraj; Yasser Yousuf Wani; Muzafar Naik
Journal:  Indian J Endocrinol Metab       Date:  2013-09
  3 in total

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