Danilo Ferreira-Moretti

Botucatu, SP, Brazil

Last Updated: 09/26/2026

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Found 18 publications

Growth Standards for Children With Smith-Magenis Syndrome (SMS).

Growth Standards for Children With Smith-Magenis Syndrome (SMS).

Journal: American journal of medical genetics. Part A

Published: February 11, 2025

DNA methylation differences in monozygotic twins with Van der Woude syndrome.

DNA methylation differences in monozygotic twins with Van der Woude syndrome.

Journal: Frontiers in dental medicine

Published: March 20, 2023

Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects.

Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects.

Journal: American journal of medical genetics. Part A

Published: December 23, 2020

Rubinstein-Taybi syndrome in diverse populations.

Rubinstein-Taybi syndrome in diverse populations.

Journal: American journal of medical genetics. Part A

Published: June 26, 2020

Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay.

Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay.

Journal: Genetics and molecular biology

Published: September 27, 2018

Are variants in sex hormone metabolizing genes associated with stuttering?

Are variants in sex hormone metabolizing genes associated with stuttering?

Journal: Brain and language

Published: August 20, 2018

Cornelia de Lange syndrome in diverse populations.

Cornelia de Lange syndrome in diverse populations.

Journal: American journal of medical genetics. Part A

Published: June 05, 2018

Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene.

Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene.

Journal: European journal of human genetics : EJHG

Published: April 27, 2018

Williams-Beuren syndrome in diverse populations.

Williams-Beuren syndrome in diverse populations.

Journal: American journal of medical genetics. Part A

Published: December 18, 2017

Incorporation of 5-ethynyl-2'-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangements.

Incorporation of 5-ethynyl-2'-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangements.

Journal: Human genetics

Published: September 30, 2015

X-linked intellectual disability related genes disrupted by balanced X-autosome translocations.

X-linked intellectual disability related genes disrupted by balanced X-autosome translocations.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: April 30, 2015

Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes.

Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes.

Journal: European journal of human genetics : EJHG

Published: February 06, 2015

Showing 1-12 of 18

Last Updated: 09/26/2026