Origins of the fragile X syndrome mutation.

Origins of the fragile X syndrome mutation.

Item
http://www.wikidata.org/entity/Q41653200
Fragile X syndromeFragile X syndrome: a review of clinical and molecular diagnoses.Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotypeTwo new cases of FMR1 deletion associated with mental impairment.Fragile X gene instability: anchoring AGGs and linked microsatellitesFragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference Lab.Diverse Profiles of Anxiety Related Disorders in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes.Fragile X syndrome in humans and mice.Screening for fragile X syndrome: information needs for health planners.Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans.Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28.Fragile X founder effects and new mutations in Finland.Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
P2860

Origins of the fragile X syndrome mutation.

Item
http://www.wikidata.org/entity/Q41653200
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Origins of the fragile X syndrome mutation.
@en
type
label
Origins of the fragile X syndrome mutation.
@en
prefLabel
Origins of the fragile X syndrome mutation.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P932
P356
P1433
P1476
Origins of the fragile X syndrome mutation.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P932