Detalhe da pesquisa
1.
Chromosome analysis of 303 pregnancy losses in Mexico.
Gac Med Mex
; 160(1): 76-85, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38753554
2.
Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensus.
Hum Mutat
; 43(12): 1732-1744, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35842788
3.
Carrier screening in the Mexican Jewish community using a pan-ethnic expanded carrier screening NGS panel.
Genet Med
; 24(4): 821-830, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34961661
4.
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.
Clin Genet
; 99(6): 823-828, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33583041
5.
Causal analysis of fetal death in high-risk pregnancies.
J Perinat Med
; 49(6): 740-747, 2021 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33735952
6.
The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread.
J Assist Reprod Genet
; 38(7): 1879-1886, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33751332
7.
Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes.
Mod Pathol
; 33(6): 1237, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32051555
8.
Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes.
Mod Pathol
; 33(5): 880-892, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31857680
9.
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients.
Mod Pathol
; 31(7): 1116-1130, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29463882
10.
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.
Prenat Diagn
; 33(3): 205-8, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23354651
11.
Heterogeneous Diagnoses Underlying Radial Ray Anomalies.
Indian J Pediatr
; 84(3): 200-205, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27987078
12.
Sonic hedgehog mutation analysis in patients with VACTERL association.
Am J Med Genet A
; 152A(3): 781-3, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20186790
13.
Anophthalmia-esophageal atresia syndrome caused by an SOX2 gene deletion in monozygotic twin brothers with markedly discordant phenotypes.
Am J Med Genet A
; 140(18): 1899-903, 2006 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16892407
14.
Paternal gonadal mosaicism detected in a couple with recurrent abortions undergoing PGD: FISH analysis of sperm nuclei proves valuable.
Reprod Biomed Online
; 9(2): 225-30, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15333256
15.
Análisis y resultados clinicocitogenéticos de fetos y recién nacidos con alteraciones cromosómicas durante un año en el Instituto Nacional de Perinatología / Analysis of clinical and cytogenetic studies fetus and new born with chromosomal anomalies during one year at the Instituto Nacional de Perinatología
Perinatol. reprod. hum
; 19(2): 94-105, abr.-jun. 2005. ilus, tab
Artigo
em Espanhol
| LILACS | ID: lil-632268
16.
Abscesos cerebrales múltiples por Actinomyces sp / Multiple cerebral abscess due to Actinomyces sp
An. méd. Asoc. Méd. Hosp. ABC
; 43(4): 174-8, oct.-dic. 1998. ilus
Artigo
em Espanhol
| LILACS | ID: lil-240954