Detalhe da pesquisa
1.
Isolated postaxial polydactyly: Epidemiologic characteristics from a multicenter birth defects study.
Am J Med Genet A
; 179(8): 1432-1441, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31091006
2.
Genetic Risk Determinants for Cigarette Smoking Dependence in Mexican Mestizo Families.
Nicotine Tob Res
; 18(5): 620-5, 2016 May.
Artigo
Inglês
| MEDLINE | ID: mdl-26416825
3.
Clinical and Genetic Findings in Mexican Patients with Duane Anomaly and Radial Ray Malformations/Okihiro Syndrome.
Rev Invest Clin
; 68(5): 269-274, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27941963
4.
Identification of Copy Number Variations in Isolated Tetralogy of Fallot.
Pediatr Cardiol
; 36(8): 1642-6, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26036351
5.
Prevalence of esophageal atresia among 18 international birth defects surveillance programs.
Birth Defects Res A Clin Mol Teratol
; 94(11): 893-9, 2012 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-22945024
6.
[Congenital malformations in the offspring of epileptic mothers with and without anticonvulsant treatment]. / Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes.
Salud Publica Mex
; 54(6): 579-86, 2012.
Artigo
Espanhol
| MEDLINE | ID: mdl-23318894
7.
Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based study.
Birth Defects Res
; 114(12): 631-644, 2022 07 15.
Artigo
Inglês
| MEDLINE | ID: mdl-35633200
8.
Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research.
Am J Med Genet C Semin Med Genet
; 157C(4): 274-87, 2011 Nov 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22002822
9.
Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review.
Am J Med Genet C Semin Med Genet
; 157C(4): 358-73, 2011 Nov 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22002878
10.
Prevalence and clinical characteristics of alpha-1 antitrypsin deficiency in liver explants in a Mexican cohort.
Clin Res Hepatol Gastroenterol
; 45(4): 101519, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-33636655
11.
A multi-country study of prevalence and early childhood mortality among children with omphalocele.
Birth Defects Res
; 112(20): 1787-1801, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33067932
12.
OEIS complex: Prevalence, clinical, and epidemiologic findings in a multicenter Mexican birth defects surveillance program.
Birth Defects Res
; 111(11): 666-671, 2019 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31042330
13.
Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families.
J Cosmet Dermatol
; 14(4): 268-73, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26178169
14.
Familial amyloidosis with polyneuropathy associated with TTR Ser50Arg mutation.
Amyloid
; 19(4): 171-6, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22928869
15.
Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes / Congenital malformations in the offspring of epileptic mothers with and without anticonvulsant treatment
Salud pública Méx
; 54(6): 579-586, nov.-dic. 2012. ilus, tab
Artigo
Espanhol
| LILACS | ID: lil-661177