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Confirmation of linkage of benign familial infantile convulsions to chromosome 16p, and indication of further genetic heterogeneity
Confirmation of linkage of benign familial infantile convulsions to chromosome 16p, and indication of further genetic heterogeneity
2004
Pmc Callenbach
E. H. van den Boogerd
Ifm de Coo
R. ten Houten
R.R. Frants
O. F. Brouwer
Amjm van den Maagdenberg
Keywords:
Genetic heterogeneity
Chromosome
Genetics
Medicine
Correction
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