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8. The CEPH consortium linkage map of human chromosome 2

9. The human loricrin gene.

11. Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

26. Localization of two genes encoding plasma membrane Ca2+ATPases isoforms 2 (ATP2B2) and 3 (ATP2B3) to human chromosomes 3p26→p25 and Xq28, respectively

29. Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11

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