A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
about
Genetics of bipolar disorderIncreased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataThe clinical impact of chromosomal microarray on paediatric care in Hong Kong.Decrease of miR-202-3p expression, a novel tumor suppressor, in gastric cancer.DSDs: genetics, underlying pathologies and psychosexual differentiation.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 geneArray-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis.Chromosome r(10)(p15.3q26.12) in a newborn child: case reportChromosome 10q26 deletion syndrome: Two new cases and a review of the literature.Ring chromosome 10: report on two patients and review of the literature.miR-202 suppresses cell proliferation in human hepatocellular carcinoma by downregulating LRP6 post-transcriptionally.Benign, Pathogenic and Copy Number Variations of Unknown Clinical Significance in Patients with Congenital Malformations and Developmental DelayTargetome profiling, pathway analysis and genetic association study implicate miR-202 in lymphomagenesis.An interstitial deletion at 10q26.2q26.3.Inverted Duplication and Deletion of 10q25q26 in a Patient without Any Obvious Skeletal Anomalies.Aetiology 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.Identification of critical regions for clinical features of distal 10q deletion syndrome.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.Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.
P2860
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P2860
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年學術文章
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name
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@en
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@nl
type
label
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@en
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@nl
prefLabel
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@en
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@nl
P2093
P356
P1476
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
@en
P2093
Jan Wauters
Liesbeth Rooms
Sarah Barbera Pera
Winnie Courtens
P304
P356
10.1002/AJMG.A.31053
P407
P577
2006-02-01T00:00:00Z