Chromosome 10q Deletion Latest Advances

Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: April 13, 2020

WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome.

Journal: European journal of medical genetics

Published: August 21, 2018

The Genomics of Prostate Cancer: emerging understanding with technologic advances.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: July 29, 2017

Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.

Journal: American journal of medical genetics. Part A

Published: June 29, 2016

10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies.

Journal: American journal of medical genetics. Part A

Published: November 18, 2014

Private rare deletions in SEC16A and MAMDC4 may represent novel pathogenic variants in familial axial spondyloarthritis.

Journal: Annals of the rheumatic diseases

Published: August 15, 2014

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas.

Journal: Genome biology

Published: July 11, 2014

Distal 10q monosomy: new evidence for a neurobehavioral condition?

Journal: European journal of medical genetics

Published: September 17, 2013

Ring chromosome 10: report on two patients and review of the literature.

Journal: Journal of applied genetics

Published: September 13, 2012

The chromosome 10q26 susceptibility locus in age-related macular degeneration.

Journal: Advances in experimental medicine and biology

Published: December 21, 2011

Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome.

Journal: American journal of medical genetics. Part A

Published: January 14, 2011

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Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion.

Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion.

WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome.

WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome.

The Genomics of Prostate Cancer: emerging understanding with technologic advances.

The Genomics of Prostate Cancer: emerging understanding with technologic advances.

Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.

Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.

10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies.

10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies.

Private rare deletions in SEC16A and MAMDC4 may represent novel pathogenic variants in familial axial spondyloarthritis.

Private rare deletions in SEC16A and MAMDC4 may represent novel pathogenic variants in familial axial spondyloarthritis.

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas.

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas.

Distal 10q monosomy: new evidence for a neurobehavioral condition?

Distal 10q monosomy: new evidence for a neurobehavioral condition?

Ring chromosome 10: report on two patients and review of the literature.

Ring chromosome 10: report on two patients and review of the literature.

The chromosome 10q26 susceptibility locus in age-related macular degeneration.

The chromosome 10q26 susceptibility locus in age-related macular degeneration.

Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome.

Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome.