Chromosome 2p Duplication Latest Advances

Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations.

Journal: Cytogenetic and genome research

Published: January 20, 2023

Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: July 20, 2016

Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor.

Journal: European journal of medical genetics

Published: June 07, 2016

Duplication 2p25 in a child with clinical features of CHARGE syndrome.

Journal: American journal of medical genetics. Part A

Published: December 17, 2015

Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.

Journal: Cytogenetic and genome research

Published: February 17, 2014

Metachronous neuroblastoma in an infant with germline translocation resulting in partial trisomy 2p: a role for ALK?

Journal: Journal of pediatric hematology/oncology

Published: November 27, 2013

Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation.

Journal: Genetic counseling (Geneva, Switzerland)

Published: September 17, 2013

Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.

Journal: Cytogenetic and genome research

Published: November 26, 2012

A new entity in WHO classification of tumors of the central nervous system--embryonic tumor with abundant neuropil and true rosettes: case report and review of literature

Journal: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Published: January 01, 2011

A case of complete trisomy 2p/triploidy mosaicism.

Journal: Acta paediatrica Scandinavica

Published: November 01, 1988

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Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations.

Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations.

Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses.

Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses.

Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor.

Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor.

Duplication 2p25 in a child with clinical features of CHARGE syndrome.

Duplication 2p25 in a child with clinical features of CHARGE syndrome.

Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.

Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.

Metachronous neuroblastoma in an infant with germline translocation resulting in partial trisomy 2p: a role for ALK?

Metachronous neuroblastoma in an infant with germline translocation resulting in partial trisomy 2p: a role for ALK?

Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation.

Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation.

Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.

Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.

A new entity in WHO classification of tumors of the central nervous system--embryonic tumor with abundant neuropil and true rosettes: case report and review of literature

A new entity in WHO classification of tumors of the central nervous system--embryonic tumor with abundant neuropil and true rosettes: case report and review of literature

A case of complete trisomy 2p/triploidy mosaicism.

A case of complete trisomy 2p/triploidy mosaicism.