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Test-merged-2
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# proj.
# Ann.
updated_at
PubMed
8944024
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colou
1.02 KB
2015-03-12
9
0
2021-12-23
PubMed
17000021
No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1
2.11 KB
2015-11-23
14
34
2021-12-23
PubMed
16970763
Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and
1.89 KB
2015-11-20
12
56
2021-12-23
PubMed
16822828
Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-perfo
1.89 KB
2015-11-23
9
39
2021-12-23
PubMed
16419642
A novel missense mutation, F826Y, in the mineralocorticoid receptor gene in Japanese hypertensives:
1.78 KB
2015-11-20
13
26
2021-12-23
PubMed
16330669
Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and
2 KB
2015-11-19
12
32
2021-12-23
PubMed
16321363
Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation. We describ
925 Bytes
2015-11-23
16
13
2021-12-23
PubMed
16001362
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nuc
2.06 KB
2015-11-19
12
38
2021-12-23
PubMed
15824163
No Evidence for BRAF as a melanoma/nevus susceptibility gene. Somatic mutations of BRAF have been id
1.75 KB
2015-11-19
12
31
2021-12-23
PubMed
15623763
TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients. PURPOSE: T
1.89 KB
2015-11-18
13
57
2021-12-23
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