PMC:1852721 / 2209-2727 JSONTXT

{"project":"2_test","denotations":[{"id":"17357067-16824022-2054032","span":{"begin":48,"end":49},"obj":"16824022"},{"id":"17357067-13932119-2054033","span":{"begin":324,"end":325},"obj":"13932119"},{"id":"17357067-14209042-2054034","span":{"begin":514,"end":515},"obj":"14209042"},{"id":"17357067-14280821-2054035","span":{"begin":517,"end":518},"obj":"14280821"}],"text":"MIM had its origins in three different endeavors3: first, the annual reviews of medical genetics that my colleagues and I in the Moore Clinic at Johns Hopkins prepared for each of 6 years, 1958–19634, 5; second, a catalog of X-linked traits that I compiled in 1962 as an assessment of the genetic content of the X chromosome6, 7; and, third, a catalog of autosomal recessive phenotypes that I prepared in 1963 as a resource for identifying both “old” and “new” recessive diseases in studies of the Old Order Amish.8, 9"}