Amiese_DoopsgesindesAmische%D8%A3%D9%85%D9%8A%D8%B4%D8%A7%D9%85%D9%8A%D8%B4Ami%C5%9F%D0%90%D0%BC%D1%96%D1%88%D1%8B%D0%90%D0%BC%D0%B8%D1%88%D0%B8AmishedAmishAmi%C5%A1ov%C3%A9AmischAmishKategorie:AmischeAmischeAmi%C5%9F%CE%86%CE%BC%CE%B9%CF%82AmishAmi%C5%9DismoAmishAmi%C5%A1idAmish%D8%A2%D9%85%DB%8C%D8%B4AmissitAmishAmishAmanaighAmish%D7%90%D7%9E%D7%99%D7%A9Ami%C5%A1iAmishokAmishAmish%E3%82%A2%E3%83%BC%E3%83%9F%E3%83%83%E3%82%B7%E3%83%A5%E1%83%90%E1%83%9B%E1%83%98%E1%83%A8%E1%83%94%E1%83%91%E1%83%98%E0%B2%85%E0%B2%AE%E0%B2%BF%E0%B2%B6%E0%B3%8D%EC%95%84%EB%AF%B8%EC%8B%9C%ED%8C%8CAmeschAnabatisme_amixAmishAmi%C5%A1ai
about
sameAs
P135
P301
Care for Amish and Mennonite children with cystic fibrosis: a case seriesA novel nemaline myopathy in the Amish caused by a mutation in troponin T1Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathyAssociations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order AmishGenetics of propionic acidemia in a Mennonite-Amish kindredLamaze Childbirth among the Amish PeopleDNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear geneA G339R mutation in the CTNS gene is a common cause of nephropathic cystinosis in the south western Ontario Amish Mennonite populationA 4-year-old Amish boy with weakness, arthritis, rash, verbal delay, and failure to thriveAmish revisited: next-generation sequencing studies of psychiatric disorders among the Plain peopleCraniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindredDWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIAIdentification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order AmishByler disease. Fatal familial intrahepatic cholestasis in an Amish kindredBeta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateArsenic exposure is associated with diminished insulin sensitivity in non-diabetic Amish adultsParkinson disease loci in the mid-western AmishGenome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease geneSharing the Load: Amish Healthcare Financing.Description of Amish Study data set.Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish.Homozygosity by descent mapping of blood pressure in the Old Order Amish: evidence for sex specific genetic architectureNicotinic acetylcholine receptor subunit variants are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study.PedHunter 2.0 and its usage to characterize the founder structure of the Old Order Amish of Lancaster County.Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.Probable cases of mast syndrome in a non-Amish familyA genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish.Extent and distribution of linkage disequilibrium in the Old Order Amish.A population-based study of parkinsonism in an Amish community.Determinants of coronary artery and aortic calcification in the Old Order Amish.Sequence variation in IGF1R is associated with differences in insulin levels in nondiabetic Old Order Amish.Circulating CD34+ Cell Count is Associated with Extent of Subclinical Atherosclerosis in Asymptomatic Amish Men, Independent of 10-Year Framingham Risk.Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community.Investigations of the Y chromosome, male founder structure and YSTR mutation rates in the Old Order Amish.Familial aggregation of tobacco use behaviors among Amish men.Persistent Staphylococcus aureus colonization is not a strongly heritable trait in Amish familiesPrimary ciliary dyskinesia in Amish communitiesDiabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study.QTL influencing blood pressure maps to the region of PPH1 on chromosome 2q31-34 in Old Order Amish.Genome-wide scan of obesity in the Old Order Amish.
P921
description
Glaubensgemeinschaft
@de
anabaptistisk kristen grupp
@sv
communauté religieuse anabaptiste
@fr
comunità religiosa
@it
etnische groep
@nl
group of traditionalist Christian church fellowships
@en
grupo etnorreligioso protestante anabaptista
@es
kristittyjen yhteisö
@fi
Συντηρητικοί χριστιανοί ομόλογοι
@el
Менонітська течія анабаптистичного походження.
@uk
name
Amanaigh
@ga
Amesch
@lb
Amiese Doopsgesindes
@af
Amisch
@cy
Amisch
@nan
Amisch
@nds
Amisch
@pdc
Amische
@de
Amische
@gsw
Amish
@da
type
label
Amanaigh
@ga
Amesch
@lb
Amiese Doopsgesindes
@af
Amisch
@cy
Amisch
@nan
Amisch
@nds
Amisch
@pdc
Amische
@de
Amische
@gsw
Amish
@da
altLabel
Aamid
@et
Amananoj
@eo
Amenité
@cs
Amische Mennoniten
@de
Amische
@cy
Amischen
@de
Amish Church
@nb
Amish Dutch
@nl
Amish People
@de
Amish
@ar
prefLabel
Amanaigh
@ga
Amesch
@lb
Amiese Doopsgesindes
@af
Amisch
@cy
Amisch
@nan
Amisch
@nds
Amisch
@pdc
Amische
@de
Amische
@gsw
Amish
@da
P1014
P2163
P227
P2347
P244
P486
P508
P6366
P646
P1014
P112
P1417
topic/Amish
P1889
P2163
P227
P2347
P244
sh85004511
P279
P31
P3221
subject/amish