Chromosome 6q Deletion Latest Advances

6q deletion in Waldenström macroglobulinaemia negatively affects time to transformation and survival.

Journal: British journal of haematology

Published: May 18, 2020

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination.

Journal: Case reports in genetics

Published: April 15, 2020

A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short-lived infant.

Journal: Journal of clinical laboratory analysis

Published: February 28, 2020

Deletion 6q Drives T-cell Leukemia Progression by Ribosome Modulation.

Journal: Cancer discovery

Published: July 30, 2017

Terminal deletion 6q syndrome with 11q partial trisomy mosaicism due to maternal balanced translocation.

Journal: Genetic counseling (Geneva, Switzerland)

Published: May 03, 2014

A de novo 0.63 Mb 6q25.1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity.

Journal: American journal of medical genetics. Part A

Published: March 29, 2014

Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q.

Journal: Ophthalmic genetics

Published: November 21, 2013

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.

Journal: Brain : a journal of neurology

Published: September 24, 2013

6q deletion detected by fluorescence in situ hybridization using bacterial artificial chromosome in chronic lymphocytic leukemia.

Journal: European journal of haematology

Published: March 27, 2013

Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.

Journal: Genetic counseling (Geneva, Switzerland)

Published: February 26, 2013

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.

Journal: Gene

Published: October 24, 2012

Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions.

Journal: Prenatal diagnosis

Published: October 16, 2012

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6q deletion in Waldenström macroglobulinaemia negatively affects time to transformation and survival.

6q deletion in Waldenström macroglobulinaemia negatively affects time to transformation and survival.

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination.

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination.

A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short-lived infant.

A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short-lived infant.

Deletion 6q Drives T-cell Leukemia Progression by Ribosome Modulation.

Deletion 6q Drives T-cell Leukemia Progression by Ribosome Modulation.

Terminal deletion 6q syndrome with 11q partial trisomy mosaicism due to maternal balanced translocation.

Terminal deletion 6q syndrome with 11q partial trisomy mosaicism due to maternal balanced translocation.

A de novo 0.63 Mb 6q25.1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity.

A de novo 0.63 Mb 6q25.1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity.

Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q.

Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q.

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.

6q deletion detected by fluorescence in situ hybridization using bacterial artificial chromosome in chronic lymphocytic leukemia.

6q deletion detected by fluorescence in situ hybridization using bacterial artificial chromosome in chronic lymphocytic leukemia.

Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.

Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.

Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions.

Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions.