Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.
about
Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music.The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Whole exome sequencing to identify genetic causes of short statureGenetic evaluation of short stature.Evidence of inbreeding depression on human height.A pilot study on collective effects of 22q13.31 deletions on gray matter concentration in schizophreniaCopy number variants in short children born small for gestational age.Copy number variants in locally raised Chinese chicken genomes determined using array comparative genomic hybridizationAnalysis of copy number variants by three detection algorithms and their association with body size in horses.De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.Explaining additional genetic variation in complex traitsCopy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarrayTowards identification of molecular mechanisms of short stature.A novel deletion of IGF1 in a patient with idiopathic short stature provides insight Into IGF1 haploinsufficiency.The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1.Copy number variants in patients with short stature.Height matters-from monogenic disorders to normal variation.Adaptive potential of genomic structural variation in human and mammalian evolution.Expanding Genetic and Functional Diagnoses of IGF1R Haploinsufficiencies.Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause.Application of Chromosomal Microarray for Evaluation of Idiopathic Short Stature in Asian Indian Children: A Pilot Study.Small de novo CNVs as biomarkers of parental exposure to low doses of ionizing radiation of caesium-137.
P2860
Q30427847-B96B58AF-D7A8-454D-96A6-AE1928B48D5DQ30429472-A16D0299-E58C-479E-BBA2-CDF8BAE68FA5Q30607430-5665094D-34E5-47FA-8C0F-63AD34AD924FQ34033624-53745B32-8A51-4356-B7F4-F11336B6F93AQ34130975-A6C1CE43-110F-402F-AD45-6D1086B50417Q34350919-DE3CF988-1002-474D-BC28-676403B4A74BQ34534743-984BAD92-2D1C-449E-87AB-444BAE309040Q34536372-491AADE0-1B68-4EF6-9D73-2E994F8D0E05Q34675355-9E6549C3-571F-4F8A-9380-14D3C8A4A033Q34832536-31BB7282-7C4F-4C52-AF09-4A642C4267A1Q35777495-0356F05E-DB1D-49DA-8666-BA00BDDC8E9AQ36264669-C88A862B-B4BB-4181-BE7B-2F86EB17E530Q36584134-8AFB4F3B-66B7-43CD-9613-663CC4A197B5Q37329242-ACD0E7EB-C280-4920-A1E4-54A45BEDC7D6Q37428944-3BF06BF1-4565-4BAB-B768-589B665FC1F3Q37578863-11111719-B640-444C-8DE9-EFD7D2B189A6Q37711793-18A82956-2E65-4366-8EB8-CDE91B6F2DF4Q38075771-85F27909-2B9F-45E9-823A-40987BFB76B2Q38499991-E8019657-03B3-47E6-9D8F-A851CED93F82Q38844094-9625CC9F-9027-459D-8063-A8693D565563Q41317384-7B640896-DB10-4245-B6D3-6F28E81588CBQ42367768-81502608-B9E7-4325-87CE-92C045591463Q50050828-9B2B1A25-45CE-4A08-8B33-BA0D1A25DF85Q52657008-0A5A1A8F-6EAE-4F10-A20B-83A27E1D975AQ55023774-2942E293-D964-407A-865B-BDE16E434F17
P2860
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.
description
2011 nî lūn-bûn
@nan
2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genome-wide association of cop ...... w-frequency genomic deletions.
@ast
Genome-wide association of cop ...... w-frequency genomic deletions.
@en
type
label
Genome-wide association of cop ...... w-frequency genomic deletions.
@ast
Genome-wide association of cop ...... w-frequency genomic deletions.
@en
prefLabel
Genome-wide association of cop ...... w-frequency genomic deletions.
@ast
Genome-wide association of cop ...... w-frequency genomic deletions.
@en
P2093
P2860
P50
P1476
Genome-wide association of cop ...... ow-frequency genomic deletions
@en
P2093
Andrew Dauber
Bai-Lin Wu
Ellen W Demerath
James G Wilson
Jerome I Rotter
Joel N Hirschhorn
Pamela J Schreiner
Stephen S Rich
Yan A Meng
Yiping Shen
P2860
P304
P356
10.1016/J.AJHG.2011.10.014
P407
P577
2011-11-23T00:00:00Z