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source ID
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# proj.
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# Ann.
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updated_at |
| PubMed |
2884570 |
An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haploty |
1.29 KB |
2015-12-03 |
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11 |
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11 |
2025-01-16
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| PubMed |
6859721 |
Absence of the seventh component of complement in a patient with chronic meningococcemia presenting |
662 Bytes |
2015-12-06 |
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12 |
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12 |
2025-01-16
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| PubMed |
1324223 |
Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel e |
1.87 KB |
2015-11-18 |
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11 |
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13 |
2025-01-16
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| PubMed |
10533068 |
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence |
1.15 KB |
2015-11-15 |
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10 |
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4 |
2025-01-16
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| PubMed |
6585184 |
Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy.
Seventy families wit |
1.19 KB |
2015-11-28 |
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11 |
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9 |
2025-01-16
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| PubMed |
122435 |
Prenatal diagnosis of Wolman disease.
Two pregnancies at risk for Wolman disease were monitored by a |
1.17 KB |
2015-11-22 |
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9 |
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4 |
2025-01-16
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| PubMed |
7795652 |
Somatic mutations in the BRCA1 gene in sporadic ovarian tumours.
The BRCA1 gene on chromosome 17q21 |
799 Bytes |
2015-11-27 |
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9 |
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9 |
2025-01-16
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| PubMed |
2180286 |
Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.
One of female MZ t |
1.69 KB |
2015-11-26 |
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17 |
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11 |
2025-01-16
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| PubMed |
1316718 |
Coincident Kaposi sarcoma and T-cell lymphoma in a patient with the Wiskott-Aldrich syndrome.
A 24 y |
1.53 KB |
2015-11-18 |
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18 |
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22 |
2025-01-16
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| PubMed |
10071185 |
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.
Dihydropyrimidin |
1.27 KB |
2015-11-02 |
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9 |
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11 |
2025-01-16
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