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European Journal of Human Genetics : EJHG|October 22, 2009
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowthValérie Malan, Suzanne Chevallier, Gwendoline Soler, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
A search for uniparental disomy in carriers of supernumerary marker chromosomesR S James, I K Temple, N R Dennis, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Prospects of carrier screening of aspartylglucosaminuria in FinlandM Hietala, K Grön, A C Syvänen, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Molecular mapping of twenty-four features of Down syndrome on chromosome 21J M Delabar, D Theophile, Z Rahmani, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Autoimmune polyglandular disease type I. Exclusion map using amplifiable multiallelic markers in a microtiter well formatJ Aaltonen, J Komulainen, A Vikman, et al.
European Journal of Human Genetics : EJHG|November 19, 2009
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndromeMarjolein H Willemsen, Bridget A Fernandez, Carlos A Bacino, et al.
European Journal of Human Genetics : EJHG|November 26, 2009
A data-driven weighting scheme for family-based genome-wide association studiesHuaizhen Qin, Tao Feng, Shuanglin Zhang, et al.
European Journal of Human Genetics : EJHG|November 26, 2009
Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosisAntonio Alcina, Sreeram V Ramagopalan, Oscar Fernández, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Ethical implications of the use of whole genome methods in medical researchJane Kaye, Paula Boddington, Jantina de Vries, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Menkes diseaseZeynep Tümer, Lisbeth B Møller
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