Search details
1.
Congenital hearing loss: a literature review of the genetic etiology in a Mexican population.
Bol Med Hosp Infant Mex
; 79(4): 206-214, 2022.
Article
in English
| MEDLINE | ID: mdl-36100214
2.
Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems.
Rev Invest Clin
; 63(6): 614-20, 2011.
Article
in English
| MEDLINE | ID: mdl-23650674
3.
X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.
Bol Med Hosp Infant Mex
; 77(4): 212-217, 2020.
Article
in English
| MEDLINE | ID: mdl-32713954
4.
Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico City.
PLoS One
; 14(1): e0208076, 2019.
Article
in English
| MEDLINE | ID: mdl-30629602
5.
Monosomy 9p24 in two non-related patients as result of a translocation (2;9). / Monosomía 9p24 secundaria a translocación (2;9) en dos pacientes no relacionadas.
Arch Argent Pediatr
; 116(4): e603-e608, 2018 08 01.
Article
in Spanish
| MEDLINE | ID: mdl-30016040
6.
[Pallister-Killian syndrome in a Mexican mestizo patient. Case report]. / Síndrome de Pallister-Killian en una paciente mestiza mexicana. Reporte de caso.
Arch Argent Pediatr
; 116(1): e135-e138, 2018 Feb 01.
Article
in Spanish
| MEDLINE | ID: mdl-29333839
7.
Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literature.
Int J Dermatol
; 56(4): 435-439, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-28217872
8.
Silver-Russell syndrome caused by trisomy 11p15.5 due to a derivative X chromosome from a de novo t(X;11) in a Mexican female patient.
Clin Dysmorphol
; 31(2): 94-97, 2022 Apr 01.
Article
in English
| MEDLINE | ID: mdl-34750319
9.
Congenital hearing loss: a literature review of the genetic etiology in a Mexican population / Pérdida auditiva congénita: revisión de la etiología genética en la población mexicana
Bol. méd. Hosp. Infant. Méx
; 79(4): 206-214, Jul.-Aug. 2022. tab
Article
in English
|
LILACS-Express
| ID: biblio-1403641
10.
Displasia ectodérmica hipohidrótica ligada al cromosoma X de novo por variante recurrente en un paciente mexicano / X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient
Bol. méd. Hosp. Infant. Méx
; 77(4): 212-217, Jul.-Aug. 2020. graf
Article
in Spanish
| LILACS | ID: biblio-1131979
11.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
BMC Med Genomics
; 7: 55, 2014 Sep 15.
Article
in English
| MEDLINE | ID: mdl-25223409
12.
Monosomía 9p24 secundaria a translocación (2; 9) en dos pacientes no relacionadas / Monosomy 9p24 in two non-related patients as result of a translocation (2; 9)
Arch. argent. pediatr
; 116(4): 603-608, ago. 2018. ilus, tab
Article
in Spanish
| LILACS, BINACIS | ID: biblio-950051
13.
Síndrome de Pallister-Killian en una paciente mestiza mexicana: Reporte de caso / Paüister-KiUian syndrome in a Mexican mestizo patient: Case report
Arch. argent. pediatr
; 116(1): 135-138, feb. 2018. ilus
Article
in Spanish
| LILACS, BINACIS | ID: biblio-887445
14.
Caudal duplication with multicystic dysplastic kidney: a case report.
Clin Dysmorphol
; 24(1): 26-8, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25304120
15.
Trascendencia de los factores ambientales y genéticos en cardiopatías congénitas: el caso de la enzima MTHFR / Significance of enviromental and genetic factors related to congenital heart diseases: MTHFR enzyme case
Perinatol. reprod. hum
; 20(1/3): 39-47, ene.-sep. 2006. ilus
Article
in Spanish
| LILACS | ID: lil-632288
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