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Comparison of Perinatal Outcomes between Patients with Suspected Complex and Simple Gastroschisis

American journal of perinatology, 2024-02, Vol.41 (3), p.282

2024

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The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread

Journal of assisted reproduction and genetics, 2021-07, Vol.38 (7), p.1879-1886

2021

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The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients

Modern pathology, 2018-07, Vol.31 (7), p.1116-1130

2018

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Carrier screening in the Mexican Jewish community using a pan-ethnic expanded carrier screening NGS panel

Genetics in medicine, 2022-04, Vol.24 (4), p.821-830

2022

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Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes

Modern pathology, 2020-05, Vol.33 (5), p.880-892

2020

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Mortality from Congenital Heart Disease in Mexico: A Problem on the Rise

PloS one, 2016-03, Vol.11 (3), p.e0150422-e0150422

2016

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Causal analysis of fetal death in high-risk pregnancies

Journal of perinatal medicine, 2021-07, Vol.49 (6), p.740-747

2021

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Clinical and genetic description of patients with prenatally identified cardiac tumors

Prenatal diagnosis, 2019-10, Vol.39 (11), p.998-1004

2019

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The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss

Prenatal diagnosis, 2013-03, Vol.33 (3), p.205-208

2013

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Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes

Modern pathology, 2020-06, Vol.33 (6), p.1237-1237

2020

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Prevalence, clinical features, and outcomes of SARS-CoV-2 infection in pregnant women with or without mild/moderate symptoms: Results from universal screening in a tertiary care center in Mexico City, Mexico

PloS one, 2021-04, Vol.16 (4), p.e0249584-e0249584

2021

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Heterogeneous Diagnoses Underlying Radial Ray Anomalies

Indian journal of pediatrics, 2017-03, Vol.84 (3), p.200-205

2017

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Sonic hedgehog mutation analysis in patients with VACTERL association

American journal of medical genetics. Part A, 2010-03, Vol.152A (3), p.781-783

2010

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Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensus

Human mutation, 2022-12, Vol.43 (12), p.1732-1744

2022

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Hyperglycemia differentially affects proliferation, apoptosis, and BNIP3 and p53 mRNA expression of human umbilical cord Wharton's jelly cells from non-diabetic and diabetic pregnancies

Biochemical and biophysical research communications, 2019-01, Vol.508 (4), p.1149-1154

2019

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Acute Abdomen in Pregnancy due to Idiopathic Chylous Ascites

Case reports in obstetrics and gynecology, 2024-02, Vol.2024, p.1-5

2024

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Amniotic band sequence: prenatal diagnosis, phenotype descriptions, and a proposal of a new classification based on morphologic findings

Revista de investigacion clinica, 2013-07, Vol.65 (4), p.300-306

2013

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Giant left ventricular rhabdomyoma treated successfully with everolimus: case report and review of literature

Cardiology in the young, 2018-07, Vol.28 (7), p.903-909

2018

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Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure

Clinical genetics, 2021-06, Vol.99 (6), p.823-828

2021

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Estudio cromosómico de 303 pérdidas gestacionales en México

Gaceta médica de México, 2024-01, Vol.160 (1), p.81-91

2024

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AZFa, AZFb, AZFc and gr/gr Y-chromosome microdeletions in azoospermic and severe oligozoospermic patients, analyzed from a neural network perspective

Cirugía y cirujanos, 2022-04, Vol.90 (2), p.202-209

2022

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Severe phenotype in two half-sibs with Adams Oliver syndrome

Archivos argentinos de pediatría, 2014-06, Vol.112 (3), p.e108-e112

2014

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Association between selected structural defects and chromosomal abnormalities

Revista de investigacion clinica, 2013-05, Vol.65 (3), p.248-254

2013

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Anophthalmia-esophageal atresia syndrome caused by an SOX2 gene deletion in monozygotic twin brothers with markedly discordant phenotypes

American journal of medical genetics. Part A, 2006-09, Vol.140A (18), p.1899-1903

2006

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Comparison of Perinatal Outcomes between Patients with Suspected Complex and Simple Gastroschisis

The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread

The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients

Carrier screening in the Mexican Jewish community using a pan-ethnic expanded carrier screening NGS panel

Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes

Mortality from Congenital Heart Disease in Mexico: A Problem on the Rise

Causal analysis of fetal death in high-risk pregnancies

Clinical and genetic description of patients with prenatally identified cardiac tumors

The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss

Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes

Prevalence, clinical features, and outcomes of SARS-CoV-2 infection in pregnant women with or without mild/moderate symptoms: Results from universal screening in a tertiary care center in Mexico City, Mexico

Heterogeneous Diagnoses Underlying Radial Ray Anomalies

Sonic hedgehog mutation analysis in patients with VACTERL association

Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensus

Hyperglycemia differentially affects proliferation, apoptosis, and BNIP3 and p53 mRNA expression of human umbilical cord Wharton's jelly cells from non-diabetic and diabetic pregnancies

Acute Abdomen in Pregnancy due to Idiopathic Chylous Ascites

Amniotic band sequence: prenatal diagnosis, phenotype descriptions, and a proposal of a new classification based on morphologic findings

Giant left ventricular rhabdomyoma treated successfully with everolimus: case report and review of literature

Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure

Estudio cromosómico de 303 pérdidas gestacionales en México

AZFa, AZFb, AZFc and gr/gr Y-chromosome microdeletions in azoospermic and severe oligozoospermic patients, analyzed from a neural network perspective

COVID-19 Infection in Pregnancy: PCR Cycle Thresholds, Placental Pathology, and Perinatal Outcomes

Severe phenotype in two half-sibs with Adams Oliver syndrome

Association between selected structural defects and chromosomal abnormalities

Anophthalmia-esophageal atresia syndrome caused by an SOX2 gene deletion in monozygotic twin brothers with markedly discordant phenotypes

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