about
The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation.Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.Aspartylglycosaminuria: a reviewGenetic basis of sitosterolemiaA missense substitution A49T in the steroid 5-alpha-reductase gene (SRD5A2) is not associated with prostate cancer in FinlandFine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communitiesNationwide cancer family ascertainment using Finnish Cancer Registry data on family names and places of birth for 35,761 prostate cancer patients.High mammographic density in women of Ashkenazi Jewish descent.Genetics of population isolates.Characterization of Finnish Mycobacterium tuberculosis isolates by spoligotyping.Biochemistry of glycosphingolipid storage disorders: implications for therapeutic interventionConfounding, ascertainment bias, and the blind quest for a genetic 'fountain of youth'.Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance.A population-based study of autosomal-recessive disease-causing mutations in a founder populationThe R304X mutation of the aryl hydrocarbon receptor interacting protein gene in familial isolated pituitary adenomas: Mutational hot-spot or founder effect?LDL-receptor gene mutations and the hypocholesterolemic response to statin therapy.Gene therapy of single-gene disorders: preface to the special section.Rare non-coding variants are associated with plasma lipid traits in a founder population.Description of four new HLA alleles in the Finnish population: A*03:283N, A*68:167, C*03:327, C*03:361.Automation of diagnostic genetic testing: mutation detection by cyclic minisequencing.
P2860
Q24538902-36D80BE7-F259-46A3-B385-F703D1433A22Q24539181-4468D570-7FC9-4170-B5D5-D550FDC6C7EDQ28077247-FE2003C9-385B-4A40-B186-15085F600D67Q28361283-1696CD97-8B0A-4679-AB33-086DE44E1CB0Q28365264-14C6372A-0D97-484E-95CE-FC84F0C4F467Q28365986-2CBDD770-8B8E-4342-9030-40AE188693DEQ30614203-C11F6573-8B1B-43AE-9D3C-D1BB3D2864F7Q33739524-763761A0-BDB8-41F2-9163-0273CB4EAA84Q34657331-04877606-7352-4F19-B697-E6597CB8A2ABQ34975257-BC25397A-0104-458F-BFED-CD23A175DB5BQ35153233-2B99FE05-16A2-4AE5-BF28-054071FCE018Q35597638-20FC0340-720B-4A68-8F1F-F0F9609EBD11Q35933901-31DF2A6D-BA01-4F6D-8443-6AFFF61F0971Q36358475-A9C331E1-FEFB-424E-AE33-99E82122AB85Q42654837-7C24705E-E0B8-44FD-9ED7-93D6748E0489Q43674536-A904A55B-9BF9-408A-882F-BFB719A67E29Q45886671-D51EC171-A909-4941-973F-7D012D4FEF49Q47143371-97D1DA09-AB46-4D88-A6E3-77B9C62CD191Q48186982-AD297DB6-7FBC-4654-9CA2-AE2E96E2B820Q50140048-E211C743-3467-4932-A35B-C4653D83C5CB
P2860
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Molecular background of the Finnish disease heritage.
@en
type
label
Molecular background of the Finnish disease heritage.
@en
prefLabel
Molecular background of the Finnish disease heritage.
@en
P2860
P1433
P1476
Molecular background of the Finnish disease heritage.
@en
P2093
Peltonen L
P2860
P304
P356
10.3109/07853899709007481
P407
P577
1997-12-01T00:00:00Z