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European Journal of Human Genetics : EJHG|May 10, 2007
Differential haplotypic expression of the interleukin-18 geneSandrine Barbaux, Odette Poirier, Tiphaine Godefroy, et al.
European Journal of Human Genetics : EJHG|June 19, 2009
Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet studyGeorg B Ehret, Ashley A O'Connor, Alan Weder, et al.
European Journal of Human Genetics : EJHG|August 27, 2009
An integrated phenomic approach to multivariate allelic associationSarah Elizabeth Medland, Michael Churton Neale
European Journal of Human Genetics : EJHG|July 23, 2009
Septo-optic dysplasiaEmma A Webb, Mehul T Dattani
European Journal of Human Genetics : EJHG|July 16, 2009
In vitro readthrough of termination codons by gentamycin in the Stüve-Wiedemann SyndromeSamuel Bellais, Carine Le Goff, Nathalie Dagoneau, et al.
European Journal of Human Genetics : EJHG|April 9, 2009
SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesionsClaire Beneteau, Hélène Cavé, Anne Moncla, et al.
European Journal of Human Genetics : EJHG|July 29, 2010
X-inactivation of HSD17B10 revealed by cDNA analysis in two female patients with 17β-hydroxysteroid dehydrogenase 10 deficiencyJudit García-Villoria, Laura Gort, Irene Madrigal, et al.
European Journal of Human Genetics : EJHG|August 12, 2010
Nicotinic α5 receptor subunit mRNA expression is associated with distant 5' upstream polymorphismsRyan M Smith, Houda Alachkar, Audrey C Papp, et al.
European Journal of Human Genetics : EJHG|October 8, 2009
Functional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defectsPaulien Smits, Sandy Mattijssen, Eva Morava, et al.
European Journal of Human Genetics : EJHG|October 8, 2009
Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populationsMuthukrishnan Eaaswarkhanth, Ikramul Haque, Zeinab Ravesh, et al.
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