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Human Molecular Genetics 19

Showing records 1 to 19 | Display all abstracts in Human Molecular Genetics

98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cui X
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Guggenheim JA; Clark R
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Kim HJ
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Cui J
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cheng CH; Jenny LA
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Terry L
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
De Carvalho Junior JRL
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Patasova K; Haarman AEG
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Chang YJ; Kong Y
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Musolf AM
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Hsu CW
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Verhoeven VJM; Klaver CCW
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Huang IW; Huang IW
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Bailey-Wilson JE
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Ragi SD; Lin CS
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Hysi PG; Williams C
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Li X; Sparrow JR
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia

Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Tsang SH
Human Molecular Genetics 2022; 31: 2438-2451

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