Alcántara-Ortigoza, M.A.; Sánchez-Verdiguel, I.; Fernández-Hernández, L.; EnrÃquez-Flores, S.; González-Núñez, A.; Hernández-MartÃnez, N.L.; Sánchez, C.; González-del Angel, A.
Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children 2021, 8, 457.
https://doi.org/10.3390/children8060457
AMA Style
Alcántara-Ortigoza MA, Sánchez-Verdiguel I, Fernández-Hernández L, EnrÃquez-Flores S, González-Núñez A, Hernández-MartÃnez NL, Sánchez C, González-del Angel A.
Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children. 2021; 8(6):457.
https://doi.org/10.3390/children8060457
Chicago/Turabian Style
Alcántara-Ortigoza, Miguel Angel, IraÃs Sánchez-Verdiguel, Liliana Fernández-Hernández, Sergio EnrÃquez-Flores, Aidy González-Núñez, Nancy Leticia Hernández-MartÃnez, Carmen Sánchez, and Ariadna González-del Angel.
2021. "Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR" Children 8, no. 6: 457.
https://doi.org/10.3390/children8060457
APA Style
Alcántara-Ortigoza, M. A., Sánchez-Verdiguel, I., Fernández-Hernández, L., EnrÃquez-Flores, S., González-Núñez, A., Hernández-MartÃnez, N. L., Sánchez, C., & González-del Angel, A.
(2021). Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children, 8(6), 457.
https://doi.org/10.3390/children8060457