Chromosome 7p Duplication Latest Advances

Rare combination in an infant patient: trisomy 7p and tetralogy of Fallot.

Journal: Cardiology in the young

Published: April 12, 2022

Chromosomal Heterogeneity of the G-401 Rhabdoid Tumor Cell Line: Unusual Partial 7p Trisomy.

Journal: Frontiers in medicine

Published: April 18, 2019

Prenatal diagnosis of a rare case of 7q11.23 duplication syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 12, 2017

Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.

Journal: Taiwanese journal of obstetrics & gynecology

Published: May 17, 2016

A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.

Journal: Genetic counseling (Geneva, Switzerland)

Published: September 10, 2015

Chromosome mis-segregation and cytokinesis failure in trisomic human cells.

Journal: eLife

Published: October 07, 2014

Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations.

Journal: Blood

Published: October 02, 2014

A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH.

Journal: Genetic counseling (Geneva, Switzerland)

Published: January 01, 2014

Clinical and molecular characterization of a second case of 7p22.1 microduplication.

Journal: American journal of medical genetics. Part A

Published: November 29, 2011

Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.

Journal: European journal of pediatrics

Published: November 09, 2011

Small duplication of chromosome (7)(p22.1p22.2) and consideration of a dup 7p syndrome critical region.

Journal: Clinical dysmorphology

Published: July 08, 2011

Interphase fluorescence in situ hybridization analysis detects a much higher rate of thyroid tumors with clonal cytogenetic deviations of the main cytogenetic subgroups than conventional cytogenetics.

Journal: Cancer genetics

Published: August 17, 2010

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Rare combination in an infant patient: trisomy 7p and tetralogy of Fallot.

Rare combination in an infant patient: trisomy 7p and tetralogy of Fallot.

Chromosomal Heterogeneity of the G-401 Rhabdoid Tumor Cell Line: Unusual Partial 7p Trisomy.

Chromosomal Heterogeneity of the G-401 Rhabdoid Tumor Cell Line: Unusual Partial 7p Trisomy.

Prenatal diagnosis of a rare case of 7q11.23 duplication syndrome

Prenatal diagnosis of a rare case of 7q11.23 duplication syndrome

Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.

Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.

A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.

A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.

Chromosome mis-segregation and cytokinesis failure in trisomic human cells.

Chromosome mis-segregation and cytokinesis failure in trisomic human cells.

Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations.

Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations.

A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH.

A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH.

Clinical and molecular characterization of a second case of 7p22.1 microduplication.

Clinical and molecular characterization of a second case of 7p22.1 microduplication.

Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.

Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.

Small duplication of chromosome (7)(p22.1p22.2) and consideration of a dup 7p syndrome critical region.

Small duplication of chromosome (7)(p22.1p22.2) and consideration of a dup 7p syndrome critical region.

Interphase fluorescence in situ hybridization analysis detects a much higher rate of thyroid tumors with clonal cytogenetic deviations of the main cytogenetic subgroups than conventional cytogenetics.

Interphase fluorescence in situ hybridization analysis detects a much higher rate of thyroid tumors with clonal cytogenetic deviations of the main cytogenetic subgroups than conventional cytogenetics.