Carlos A. Vega-Venegas

Mexico, MEX, Mexico

Last Updated: 09/26/2026

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Found 10 publications

Severe Thrombocytopenia and Facial Asymmetry in a Mexican Patient with Noonan Syndrome-Like Disorder with Loose Anagen Hair: Clinical Observations and Diagnostic Considerations.

Severe Thrombocytopenia and Facial Asymmetry in a Mexican Patient with Noonan Syndrome-Like Disorder with Loose Anagen Hair: Clinical Observations and Diagnostic Considerations.

Journal: Molecular syndromology

Published: December 09, 2025

An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome.

An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome.

Journal: Journal of autism and developmental disorders

Published: August 20, 2020

Familial mesial temporal lobe epilepsy in Mexico: Inheritance pattern and clinical features.

Familial mesial temporal lobe epilepsy in Mexico: Inheritance pattern and clinical features.

Journal: Epilepsy research

Published: March 20, 2020

Further definition of the proximal 19p13.3 microdeletion/microduplication syndrome and implication of PIAS4 as the major contributor.

Further definition of the proximal 19p13.3 microdeletion/microduplication syndrome and implication of PIAS4 as the major contributor.

Journal: Clinical genetics

Published: July 29, 2019

Cognitive, Behavioral, and Adaptive Profiles in Williams Syndrome With and Without Loss of GTF2IRD2.

Cognitive, Behavioral, and Adaptive Profiles in Williams Syndrome With and Without Loss of GTF2IRD2.

Journal: Journal of the International Neuropsychological Society : JINS

Published: October 31, 2018

Influence of obesity, parental history of diabetes, and genes in type 2 diabetes: A case-control study.

Influence of obesity, parental history of diabetes, and genes in type 2 diabetes: A case-control study.

Journal: Scientific reports

Published: March 19, 2018

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.

Journal: European journal of human genetics : EJHG

Published: October 12, 2014

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype.

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype.

Journal: Molecular cytogenetics

Published: April 26, 2014

Impact of gene dosage on gene expression, biological processes and survival in cervical cancer: a genome-wide follow-up study.

Impact of gene dosage on gene expression, biological processes and survival in cervical cancer: a genome-wide follow-up study.

Journal: PloS one

Published: December 06, 2013

Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.

Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.

Journal: BioMed research international

Published: October 26, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026