Doris Pinto‐Escalante

A new case of Klippel-Trenaunay-Weber (KTW) syndrome: Evidence of autosomal dominant inheritance

José M. Ceballos-Quintal, Doris Pinto‐Escalante, Ileana Castillo‐Zapata · American Journal of Medical Genetics · 1996 · 70 citations · Full text

Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico

Lízbeth González-Herrera, María Guadalupe García‐Escalante, Ileana Castillo‐Zapata et al. · Clinical Genetics · 2002 · 45 citations

Genetic variation of <i>FTO</i>: <i>rs1421085 T&gt;C, rs8057044 G&gt;A, rs9939609 T</i>&gt;<i>A</i>, and copy number (CNV) in Mexican Mayan school‐aged children with obesity/overweight and with normal weight

Lízbeth González-Herrera, Jorge Zavala‐Castro, Claudia Ayala‐Cáceres et al. · American Journal of Human Biology · 2018 · 31 citations

Cardiometabolic Risk, Genetics, Genetic Epidemiology +24

A1298C polymorphism of the <i>MTHFR</i> gene and neural tube defects in the state of Yucatan, Mexico

Lízbeth González-Herrera, Ileana Castillo‐Zapata, María Guadalupe García‐Escalante et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2007 · 22 citations · Full text

<i>Paraoxonase 1</i> polymorphisms and haplotypes and the risk for having offspring affected with spina bifida in Southeast Mexico

Lízbeth González-Herrera, Ricardo M. Cerda‐Flores, Marianne Soledad Luna-Rivero et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2010 · 13 citations