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European Journal of Human Genetics : EJHG|October 22, 1998
Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research GroupG M Terwindt, R A Ophoff, J Haan, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasiaE Mornet, A Taillandier, S Peyramaure, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Genetic diversity in northern Spain (Basque Country and Cantabria): GM and KM variation related to demographic historiesE Esteban, J M Dugoujon, E Guitard, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathyJ Laporte, C Guiraud-Chaumeil, S M Tanner, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Crossing over analysis at pachytene in manA L Barlow, M A HulténEuropean Journal of Human Genetics : EJHG|October 22, 1998
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24A J van der Vleuten, C M van Ravenswaaij-Arts, C J Frijns, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan geneA Lasa, F Piccolo, C de Diego, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Refined mapping of the gene encoding the p127 kDa UV-damaged DNA-binding protein (DDB1) within 11q12-q13.1 and its exclusion in Best's vitelliform macular dystrophyH Stöhr, A Marquardt, A Rivera, et al.European Journal of Human Genetics : EJHG|October 22, 1998
A very high density microsatellite map (1 STR/41 kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical regionT C Cox, L L Cox, A BallabioEuropean Journal of Human Genetics : EJHG|October 22, 1998
Evidence against a major role of PEG1/MEST in Silver-Russell syndromeA M Riesewijk, N Blagitko, A A Schinzel, et al.Pageof 563