scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1038400555 |
P356 | DOI | 10.1007/BF00202869 |
P698 | PubMed publication ID | 8045567 |
P50 | author | Susana Balcells | Q43100576 |
D Grinberg | Q71585921 | ||
P2093 | author name string | M Baiget | |
R Gonzàlez-Duarte | |||
I Martínez | |||
M Bayés | |||
D Valverde | |||
L Vilageliu | |||
P2860 | cites work | Strategies for multilocus linkage analysis in humans | Q27860521 |
A simple salting out procedure for extracting DNA from human nucleated cells | Q27861086 | ||
A second-generation linkage map of the human genome | Q33192755 | ||
Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis | Q35199356 | ||
Visual arrestin interaction with rhodopsin. Sequential multisite binding ensures strict selectivity toward light-activated phosphorylated rhodopsin. | Q42623057 | ||
Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map. | Q48118575 | ||
The CEPH consortium linkage map of human chromosome 2 | Q58673615 | ||
Deficiencies in sight with the candidate gene approach | Q59012185 | ||
Assignment of the S-antigen gene (SAG) to human chromosome 2q24-q37 | Q68774905 | ||
P433 | issue | 2 | |
P304 | page(s) | 193-194 | |
P577 | publication date | 1994-08-01 | |
P1433 | published in | Human Genetics | Q5937167 |
P1476 | title | Genetic fine localization of the arrestin (S-antigen) gene 4 cM distal from D2S172 | |
P478 | volume | 94 |
Q24337358 | A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese |
Q33680206 | A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33. |
Q41652312 | Identification of genes causing photoreceptor degenerations leading to blindness |
Q28293710 | Oguchi disease: suggestion of linkage to markers on chromosome 2q |
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