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European Journal of Human Genetics : EJHG|May 11, 1999
Rapid and efficient ATM mutation detection by fluorescent chemical cleavage of mismatch: identification of four novel mutationsL Izatt, C Vessey, S V Hodgson, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French-German populationL Correa-Cerro, G Wöhr, J Häussler, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian familiesS D'Alfonso, L Nisticò, P Zavattari, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: molecular survey by regionsL R Desviat, B Pérez, A Gámez, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Dopamine D4 receptor polymorphism and idiopathic Parkinson's diseaseM F Kronenberg, H J Menzel, G Ebersbach, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Apolipoprotein E and herpes virus diseases: herpes simplex keratitisW R Lin, A B Tullo, R F Itzhaki
European Journal of Human Genetics : EJHG|October 20, 2000
The IL9R region contribution in asthma is supported by genetic association in an isolated populationP Kauppi, T Laitinen, V Ollikainen, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutationsM Witsch-Baumgartner, E Ciara, J Löffler, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
European Journal of Human Genetics : EJHG|November 22, 2017
Exome Pool-Seq in neurodevelopmental disordersBernt Popp, Arif B Ekici, Christian T Thiel, et al.
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