Alicia Cervantes

Mexico City, DIF 04960, Mexico

Last Updated: 09/26/2026

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Found 15 publications

Viral Hepatitis in Pregnant Mexican Women: Its Impact in Mother-Child Binomial Health and the Strategies for Its Eradication.

Viral Hepatitis in Pregnant Mexican Women: Its Impact in Mother-Child Binomial Health and the Strategies for Its Eradication.

Journal: Pathogens (Basel, Switzerland)

Published: July 05, 2024

Which Side of the Coin Are You on Regarding Possible Postnatal Oogenesis?

Which Side of the Coin Are You on Regarding Possible Postnatal Oogenesis?

Journal: Archives of medical research

Published: June 30, 2024

X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.

X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.

Journal: Boletin medico del Hospital Infantil de Mexico

Published: July 28, 2020

Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.

Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.

Journal: Molecular genetics & genomic medicine

Published: June 03, 2020

Liver disease in pregnancy: Medical aspects and their implications for mother and child.

Liver disease in pregnancy: Medical aspects and their implications for mother and child.

Journal: Annals of hepatology

Published: March 11, 2019

Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.

Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.

Journal: Annals of hepatology

Published: June 20, 2018

Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.

Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.

Journal: Ophthalmic genetics

Published: September 19, 2017

Monosomy 9p24 in two non-related patients as result of a translocation (2;9).

Monosomy 9p24 in two non-related patients as result of a translocation (2;9).

Journal: Archivos argentinos de pediatria

Published: September 11, 2017

Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia.

Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia.

Journal: Journal of the European Academy of Dermatology and Venereology : JEADV

Published: January 04, 2017

Congenital hypertrichosis universalis in Mexican female twins.

Congenital hypertrichosis universalis in Mexican female twins.

Journal: International journal of dermatology

Published: April 30, 2015

Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.

Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.

Journal: Archives of medical research

Published: March 04, 2015

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

Showing 1-12 of 15

Last Updated: 09/26/2026