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Aliska M Berry

Showing results (1-10 of 4) with videos related to

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Prenatal Diagnosis|January 17, 2022
Underlying genetic etiologies of congenital diaphragmatic herniaDaryl A Scott, Yoel Gofin, Aliska M Berry, et al.
Human Molecular Genetics|March 31, 2023
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Human Mutation|January 30, 2022
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiencyYoel Gofin, Tianyun Wang, Madelyn A Gillentine, et al.
American Journal of Medical Genetics. Part A|July 29, 2022
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER dataAmy Hardcastle, Aliska M Berry, Ian M Campbell, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Prenatal Diagnosis|January 17, 2022
Underlying genetic etiologies of congenital diaphragmatic herniaDaryl A Scott, Yoel Gofin, Aliska M Berry, et al.
Human Molecular Genetics|March 31, 2023
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Human Mutation|January 30, 2022
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiencyYoel Gofin, Tianyun Wang, Madelyn A Gillentine, et al.
American Journal of Medical Genetics. Part A|July 29, 2022
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER dataAmy Hardcastle, Aliska M Berry, Ian M Campbell, et al.
Pageof 1