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American_Journal
Documents
(145)
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# proj.
# Ann.
updated_at
PMC
2668026
Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and A
15.9 KB
2020-09-15
5
-
PMC
2681008
Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in
14.6 KB
2020-09-15
5
-
PMC
2694971
Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 C
25.8 KB
2020-09-15
5
-
PMC
1271393
The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L
64.3 KB
2020-12-30
4
-
PMC
2495071
HLA-DRB1∗0401 and HLA-DRB1∗0408 Are Strongly Associated with the Development of Antibodies against I
36.8 KB
2020-12-30
4
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PMC
2668061
The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, an
32.7 KB
2020-12-30
4
-
PMC
2495064
Pathogenic Mitochondrial DNA Mutations Are Common in the General Population Abstract Mitochondrial
17.4 KB
2020-12-30
4
-
PMC
1852721
Mendelian Inheritance in Man and Its Online Version, OMIM Last year marked the 40th anniversary of
77.9 KB
2020-12-30
4
-
PMC
2725236
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment Abstract Specific la
31.4 KB
2020-12-30
4
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PMC
2775821
Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfec
15.5 KB
2020-09-15
4
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