Search details
1.
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Genet Med
; 18(4): 364-71, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26226137
2.
ALOX5, LPA, MMP9 and TPO gene polymorphisms increase atherothrombosis susceptibility in middle-aged Mexicans.
R Soc Open Sci
; 7(1): 190775, 2020 Jan.
Article
in English
| MEDLINE | ID: mdl-32218930
3.
Correction to 'ALOX5, LPA, MMP9 and TPO gene polymorphisms increase atherothrombosis susceptibility in middle-aged Mexicans'.
R Soc Open Sci
; 7(2): 200167, 2020 Feb.
Article
in English
| MEDLINE | ID: mdl-32257362
4.
Unique spectrum of GJB2 mutations in Mexico.
Int J Pediatr Otorhinolaryngol
; 76(11): 1678-80, 2012 Nov.
Article
in English
| MEDLINE | ID: mdl-22925408
5.
[Capillary electrophoresis, a new diagnostic tool]. / La electroforesis capilar como una nueva estrategia en la medicina y el diagnóstico clínico.
Rev Med Chil
; 137(7): 946-56, 2009 Jul.
Article
in Spanish
| MEDLINE | ID: mdl-19802425
6.
Capillary electrophoresis for the detection of PMP22 gene duplication: study in Mexican patients.
Electrophoresis
; 29(7): 1582-4, 2008 Apr.
Article
in English
| MEDLINE | ID: mdl-18318003
Results
1 -
6
de 6
1
Next >
>>