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1.
A comparative study of structural variant calling in WGS from Alzheimer's disease families.
Life Sci Alliance
; 7(5)2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38418088
2.
Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.
Sci Rep
; 9(1): 14166, 2019 10 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31578364
3.
Author Correction: Variabilities in retinal function and structure in a canine model of cone-rod dystrophy associated with RPGRIP1 support multigenic etiology.
Sci Rep
; 8(1): 13058, 2018 Aug 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-30139995
4.
Variabilities in retinal function and structure in a canine model of cone-rod dystrophy associated with RPGRIP1 support multigenic etiology.
Sci Rep
; 7(1): 12823, 2017 10 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-28993665
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