Human molecular genetics

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.

Serotonin receptor 1c gene assigned to X chromosome in human (band q24) and mouse (bands D-F4).

Serotonin receptor 1c gene assigned to X chromosome in human (band q24) and mouse (bands D-F4).

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