Cristiano L. Ribeiro

Goiania, GO, Brazil

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications

Genomic variations in patients with myelodysplastic syndrome and karyotypes without numerical or structural changes.

Genomic variations in patients with myelodysplastic syndrome and karyotypes without numerical or structural changes.

Journal: Scientific reports
Published: September 08, 2020

Copy Number Gain at Xq28 in a Child with Global Developmental Delay Associated with a Variant Form of Hoyeraal-Hreidarsson Syndrome.

Copy Number Gain at Xq28 in a Child with Global Developmental Delay Associated with a Variant Form of Hoyeraal-Hreidarsson Syndrome.

Journal: Molecular syndromology
Published: March 18, 2019

A rare case of a boy with de novo microduplication at 5q35.2q35.3 from central Brazil.

A rare case of a boy with de novo microduplication at 5q35.2q35.3 from central Brazil.

Journal: Genetics and molecular research : GMR
Published: January 28, 2017

Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil.

Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil.

Journal: Molecular syndromology
Published: January 02, 2017

The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology.

The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology.

Journal: BioMed research international
Published: December 18, 2015

Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches.

Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches.

Journal: Genetics and molecular research : GMR
Published: April 14, 2015

A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach.

A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach.

Journal: Molecular cytogenetics
Published: March 10, 2014

Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil.

Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil.

Journal: PloS one
Published: January 30, 2014

Do GSTT1 and GSTM1 polymorphisms influence intoxication events in individuals occupationally exposed to pesticides?

Do GSTT1 and GSTM1 polymorphisms influence intoxication events in individuals occupationally exposed to pesticides?

Journal: Environmental science and pollution research international
Published: August 31, 2013

Cytogenetic damage in the buccal epithelium of Brazilian aviators occupationally exposed to agrochemicals.

Cytogenetic damage in the buccal epithelium of Brazilian aviators occupationally exposed to agrochemicals.

Journal: Genetics and molecular research : GMR
Published: December 24, 2011
Showing 1-10 of 10

Last Updated: 09/26/2026