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1 and phased haplotypes in people of Amish and Mennonite ancestry.
2 P, and I268T, the last found in a patient of Mennonite ancestry.
3                                     Affected Mennonite and Dutch patients were homozygous and doubly
4 ypical early-onset torsion dystonia of Swiss-Mennonite and non-Jewish Russian origin, respectively, t
5 a group of seven distantly related Old Order Mennonite children.
6 mutation is estimated to be present on 3% of Mennonite chromosomes and the disease affects 0.1% of th
7 of mental illnesses in traditional Amish and Mennonite communities--known collectively as the Plain p
8 elG, p.Glu117LysFS; n = 133) among Old Order Mennonites dating to 1727.
9  prominent cranial-cervical ITD in two large Mennonite families to chromosome 8.
10  a mutation in the THAP1 gene in three Amish-Mennonite families with mixed-onset primary torsion dyst
11 ia; a founder mutation was detected in Amish-Mennonite families, and a different mutation was identif
12                     In an extended Old Order Mennonite family cohort, we identified a rare missense v
13       We identified 11 members of a Canadian Mennonite family suffering from adult onset, slowly prog
14 ducted a genome-wide association study in 43 Mennonite family trios using 2,083 microsatellites and s
15 molecular studies have been conducted on the Mennonite family with X-linked mental retardation (XLMR)
16              The patient came from an inbred Mennonite family, and though the mutation identified her
17                     One family had the Amish-Mennonite founder mutation, whereas the other eight fami
18 unds (Amish-Swiss from United States, n = 8; Mennonite-German from Canada, n = 1; mixed European from
19                                              Mennonite GSD6 was linked to the PYGL locus with a multi
20                                We analyzed a Mennonite kindred with an autosomal recessive form of GS
21 dy recruiting participants from an Old Order Mennonite (OOM) community, a traditional farm lifestyle
22 nd metabolome composition in rural Old Order Mennonite (OOM) infants at low risk and Rochester, NY ur
23                   We studied a 13-generation Mennonite pedigree with autosomal recessive myopathy and