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Last Updated: 10/31/2025

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Found 38 publications

New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.

New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.

Journal: Italian journal of pediatrics
Published: August 08, 2022

Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report.

Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report.

Journal: European journal of medical research
Published: March 16, 2021

A rare chromosomal disorder in a newborn: Trisomy 3q.

A rare chromosomal disorder in a newborn: Trisomy 3q.

Journal: The Turkish journal of pediatrics
Published: January 18, 2020

Prenatal diagnosis of partial trisomy 3q in a fetus

Prenatal diagnosis of partial trisomy 3q in a fetus

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 11, 2019

Prenatal identification of partial 3q duplication syndrome.

Prenatal identification of partial 3q duplication syndrome.

Journal: BMC medical genomics
Published: August 15, 2018

Distal trisomy 3q as a risk factor for neural tube defects.

Distal trisomy 3q as a risk factor for neural tube defects.

Journal: Taiwanese journal of obstetrics & gynecology
Published: July 27, 2016

PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN

PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN

Journal: Akusherstvo i ginekologiia
Published: July 04, 2015

Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.

Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.

Journal: Taiwanese journal of obstetrics & gynecology
Published: October 14, 2014

A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.

A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.

Journal: Gene
Published: July 26, 2013

3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.

3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.

Journal: Gene
Published: July 23, 2013

Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.

Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.

Journal: Gene
Published: October 31, 2012

Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype.

Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype.

Journal: Genetic counseling (Geneva, Switzerland)
Published: August 19, 2011
Showing 1-12 of 38

Last Updated: 10/31/2025