Concepedia
1
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130
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H-Index
1994
Active since
Affiliations
Centre For Human Genetics(Current)
Henk Meljer is an author at Centre For Human Genetics.
Publications per year
1994–1994
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome
Henk Meljer, Esther de Graaff, Diane M.L. Merckx et al. · Human Molecular Genetics · 1994 · 130 citations
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