Browsing by Author Figuera, LE

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 20 of 22  next >
TitleAuthor(s)???itemlist.dc.contributor.other??????itemlist.dc.contributor.editor???
Are hypotrichosis simplex and monilethrix allelle forms?: Description of a Mexican family.Davalos, N; Davalos, IP; Patino-Garcia, B; Garcia-Vargas, A; Tarango-Martinez, V; Sanchez-Castellanos, ME; Villarreal, I; Garcia-Cruz, D; Feria-Velazco, A; Cantu, JM; Figuera, LE--
Are hypotrichosis simplex and monilethrix allelle forms?: Description of a Mexican family.Davalos, N; Davalos, IP; Patino-García, B; García-Vargas, A; Tarango-Martinez, V; Sanchez-Castellanos, ME; Villarreal, I; García-Cruz, D; Feria-Velazco, A; Cantu, JM; Figuera, LE--
Association of beta-defensin 1 single nucleotide polymorphisms with atopic dermatitisde Oca, EPM; Garcia-Vargas, A; Lozano-Inocencio, R; Gallegos-Arreola, MP; Sandoval-Ramirez, L; Davalos-Rodriguez, NO; Figuera, LE--
Association of beta-defensin 1 single nucleotide polymorphisms with atopic dermatitisde Oca, EPM; García-Vargas, A; Lozano-Inocencio, R; Gallegos-Arreola, MP; Sandoval-Ramirez, L; Davalos-Rodriguez, NO; Figuera, LE--
Association of genetic polimorphysm APOB (VNTR) in patients with isquemic cardiomyopathy of Mexican population.Gallegos, MP; Rangel, H; Zuniga, M; Arnaud, L; Lopez, L; Figuera, LE; Beltran, TJ; Arechavaleta, MR; Sandoval, L; Zuniga, GM--
Association of genetic polimorphysm APOB (VNTR) in patients with isquemic cardiomyopathy of Mexican population.Gallegos, MP; Rangel, H; Zuniga, M; Arnaud, L; Lopez, L; Figuera, LE; Beltran, TJ; Arechavaleta, MR; Sandoval, L; Zuniga, GM--
Deletion 13q and skeletal dysplasia in a Mexican patient.Morales, JA; Macias, NM; Wong-Ley, LE; Gallegos-Arreola, MP; Vasquez, AI; Figuera, LE--
Deletion 13q and skeletal dysplasia in a Mexican patient.Morales, JA; Macias, NM; Wong-Ley, LE; Gallegos-Arreola, MP; Vasquez, AI; Figuera, LE--
Frequency of Pvull (LPL) genetic polymorphism in patients with Arterial Coronary Disease from Mexican population.Arnaud, L; Gallegos, MP; Mariaud, RP; Ramirez, LJ; Figuera, LE; Ventura, AJ; Gaxiola, R; Beltran, TJ; Zuniga, GM--
Frequency of Pvull (LPL) genetic polymorphism in patients with Arterial Coronary Disease from Mexican population.Arnaud, L; Gallegos, MP; Mariaud, RP; Ramirez, LJ; Figuera, LE; Ventura, AJ; Gaxiola, R; Beltran, TJ; Zuniga, GM--
Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRsRangel-Villalobos, H; Rivas, F; Sandoval, L; Ibarra, B; García-Carvajal, ZY; Cantu, JM; Figuera, LE--
Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRsRangel-Villalobos, H; Rivas, F; Sandoval, L; Ibarra, B; Garcia-Carvajal, ZY; Cantu, JM; Figuera, LE--
Heteroallelic monozygotic twins and tripletsCantu, JM; Diaz-Gallardo, MY; Barros-Nunez, P; Figuera, LE--
Heteroallelic monozygotic twins and tripletsCantu, JM; Diaz-Gallardo, MY; Barros-Nunez, P; Figuera, LE--
Infantile Systemic Hyalinosis in a patient with chromosome 22 inversion.Marcias-Gomez, N; Arnaud, L; Nastasi, JA; Duran, J; Gomez-Sanchez, H; Davalos-Pulido, RM; Vasquez, AI; Garcia-Ortiz, JE; Gallegos-Arreola, MP; Figuera, LE--
Infantile Systemic Hyalinosis in a patient with chromosome 22 inversion.Marcias-Gomez, N; Arnaud, L; Nastasi, JA; Duran, J; Gomez-Sanchez, H; Davalos-Pulido, RM; Vasquez, AI; García-Ortiz, JE; Gallegos-Arreola, MP; Figuera, LE--
Inherited hypertrichosesGarcia-Cruz, D; Figuera, LE; Cantu, JM--
Inherited hypertrichosesGarcía-Cruz, D; Figuera, LE; Cantu, JM--
Punctata Keratoderma and gastrointestinal malignancy in a Mexican family.Davalos, N; Ruiz, M; Garcia-Vargas, A; Davajos, IP; Garcia-Cruz, D; Figuera, LE--
Punctata Keratoderma and gastrointestinal malignancy in a Mexican family.Davalos, N; Ruiz, M; García-Vargas, A; Davajos, IP; García-Cruz, D; Figuera, LE--