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NCBI-Disease-Corpus-high-o3-2
Documents
(100)
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# proj.
# Ann.
updated_at
PubMed
9288106
Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia. A
1.74 KB
2015-11-27
28
18
2025-03-13
PubMed
9294109
Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal
1.33 KB
2015-12-08
45
2
2025-03-13
PubMed
9311732
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma. In most patie
2.03 KB
2015-11-27
24
5
2025-03-13
PubMed
932197
Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and
2 KB
2015-12-04
27
7
2025-03-13
PubMed
9336417
Susceptibility to ankylosing spondylitis in twins: the role of genes, HLA, and the environment. OBJE
1.66 KB
2015-03-12
23
7
2025-03-13
PubMed
9342365
Cell cycle-dependent colocalization of BARD1 and BRCA1 proteins in discrete nuclear domains. Germ-li
1.39 KB
2015-03-12
22
1
2025-03-13
PubMed
9358014
Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism. Recent studies have shown that hered
1.03 KB
2015-11-28
24
5
2025-03-13
PubMed
9360520
Autosomal dominant neurohypophyseal diabetes insipidus associated with a missense mutation encoding
1.31 KB
2015-11-27
27
5
2025-03-13
PubMed
9371490
Frequent inactivation of PTEN/MMAC1 in primary prostate cancer. Sporadic prostate carcinoma is the m
1.14 KB
2015-11-27
23
5
2025-03-13
PubMed
9382108
Risk reversals in predictive testing for Huntington disease. The first predictive testing for Huntin
1 KB
2015-03-12
28
5
2025-03-13
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