Zivile Ciuladaite

Santariškių St. 2
Vilnius, VL LT08661, Lithuania

Last Updated: 09/26/2026

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Found 10 publications

Clinical, cytogenetic and molecular study of a case of ring chromosome 10.

Clinical, cytogenetic and molecular study of a case of ring chromosome 10.

Journal: Molecular cytogenetics

Published: January 07, 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

Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.

Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.

Journal: Cytogenetic and genome research

Published: July 14, 2014

Considering specific clinical features as evidence of pathogenic copy number variants.

Considering specific clinical features as evidence of pathogenic copy number variants.

Journal: Journal of applied genetics

Published: November 17, 2013

Familial distal monosomy 5p15.3-pter with trisomy 12q24.2-qter resulting in neurodevelopmental delay and dysmorphic features.

Familial distal monosomy 5p15.3-pter with trisomy 12q24.2-qter resulting in neurodevelopmental delay and dysmorphic features.

Journal: Journal of child neurology

Published: January 24, 2013

Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis.

Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis.

Journal: Cytogenetic and genome research

Published: July 09, 2012

A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability.

A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability.

Journal: American journal of medical genetics. Part A

Published: January 03, 2012

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

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

Journal: American journal of medical genetics. Part A

Published: November 29, 2011

A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features.

A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features.

Journal: European journal of medical genetics

Published: October 31, 2011

De novo 5q35.5 duplication with clinical presentation of Sotos syndrome.

De novo 5q35.5 duplication with clinical presentation of Sotos syndrome.

Journal: American journal of medical genetics. Part A

Published: October 15, 2011

Showing 1-10 of 10

Last Updated: 09/26/2026