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Human Molecular Genetics 22
Showing records 1 to 22 | Display all abstracts in Human Molecular Genetics98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Guggenheim JA
Human Molecular Genetics 2022; 31: 1909-1919
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
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
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
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
Patasova K
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; Chang YJ
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
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
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; Verhoeven VJM
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; 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
Klaver CCW; 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
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
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
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
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