Identification of critical regions for clinical features of distal 10q deletion syndrome.
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Genetics of bipolar disorderPrenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype.Genomic studies in fragile X premutation carriers.Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulationContribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients.Mild Phenotype in a Patient with a De Novo 6.3 Mb Distal Deletion at 10q26.2q26.3.A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible geneChromosome 10q26 deletion syndrome: Two new cases and a review of the literature.Ring chromosome 10: report on two patients and review of the literature.Aortic dilation, genetic testing, and associated diagnoses.Identification of the sex-determining region in flathead grey mullet (Mugil cephalus).Angelman Syndrome due to familial translocation: unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization.Clinical, cytogenetic and molecular study of a case of ring chromosome 10.Characterization by microarray and meiotic segregation study of a der(10)t(10;18) in a patient with infertility and normal phenotypeAetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children.Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion.Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.Molecular and clinical analyses with neuropsychological assessment of a case of del(10)(q26.2qter) without intellectual disability: Genomic and transcriptomic combined approach and review of the literature.An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.
P2860
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P2860
Identification of critical regions for clinical features of distal 10q deletion syndrome.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@en
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@nl
type
label
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@en
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@nl
prefLabel
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@en
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@nl
P2093
P1433
P1476
Identification of critical regions for clinical features of distal 10q deletion syndrome.
@en
P2093
A C Chinault
B Nowakowska
C E Keegan
D A Peiffer
J Schuette
K L Gunderson
S A Yatsenko
P2860
P356
10.1111/J.1399-0004.2008.01115.X
P577
2009-06-22T00:00:00Z