Suchergebnisse - "Ordaz-Robles, Thania"

PubPharm (4)

1

The muscle regeneration marker FOXP3 is associated with muscle injury in Duchenne muscular dystrophy

enthalten in: Brain & development | 2024

von Yannin Hernández-de la Cruz, S. | Ordaz-Robles, T. | Antonio Villaldama-Soriano, M. | +9

2

Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability

enthalten in: American journal of medical genetics. Part A | 2020

von Chacon-Camacho, O. | Arce-Gonzalez, R. | Ordaz-Robles, T. | +3

3

Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability

enthalten in: American Journal of Medical Genetics Part C: Seminars in Medical Genetics | 2020

von Chacon‐Camacho, O. | Arce‐Gonzalez, R. | Ordaz‐Robles, T. | +3

4

Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis : Surgical Treatment and Genetic Analysis

enthalten in: The American journal of case reports | 2019

von Córdoba, A. | Graue-Hernández, E. | Navas, A. | +7

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