Metabuscador

Frecuencia de mosaicismos de baja proporción del cromosoma x en parejas con antecedente de aborto recurrente

por Forero C., Maribel, Lucena Q, Elkin, Esteban Pérez, Clara
Publicado 2010

The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review

por Cárdenas Nieto , Diana, Forero Castro , Maribel, Esteban Pérez, Clara, Martínez Lozano , Julio, Briceño Balcázar , Ignacio
Publicado 8/4/

THBD sequence variants potentially related to recurrent pregnancy loss

por Quintero-Ronderos, Paula, Mercier, Eric, Gris, Jean-Christophe, Esteban-Perez, Clara, Moreno-Ortiz, Harold, Lucena, Elkin, Vaiman, Daniel, Fonseca-Mendoza, Dora Janeth, Laissue, Paul
Publicado 2017

BMP15 c.-9C>G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure

por Fonseca-Mendoza, Dora Janeth, Laissue, Paul, Ortega-Recalde, Oscar, Esteban-Perez, Clara, Moreno-Ortiz, Harold, Patiño, Liliana Catherine, Bermúdez, Olga María, Ortiz, Angela María, Restrepo, Carlos M., Lucena, Elkin
Publicado 2014

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

por Quintero-Ronderos, Paula, Jiménez, Karen Marcela, Esteban-Pérez, Clara, Ojeda, Diego A., Bello, Sandra, Coronel, María Alejandra, Moreno-Ortiz, Harold, Sierra-Díaz, Diana Carolina, Lucena, Elkin, Barbaux, Sandrine, Vaiman, Daniel, Fonseca-Mendoza, Dora Janeth, Laissue, Paul
Publicado 2019