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# proj.
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# Ann.
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updated_at |
| 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 |
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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 |
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| PubMed |
1323345 |
Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amp |
1.4 KB |
2015-11-18 |
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11 |
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5 |
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| PubMed |
2828430 |
Homozygous hypobetalipoproteinemia: a disease distinct from abetalipoproproteinemia at the molecular |
1.13 KB |
2015-11-27 |
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18 |
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9 |
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| PubMed |
10471457 |
A population-based study of the clinical expression of the hemochromatosis gene.
BACKGROUND AND METH |
2.3 KB |
2015-11-15 |
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11 |
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14 |
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| PubMed |
9949209 |
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a regi |
1.49 KB |
2015-11-27 |
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41 |
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17 |
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| PubMed |
7574457 |
Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease.
Pelizaeus-Me |
1.4 KB |
2015-11-27 |
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8 |
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6 |
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| PubMed |
8808605 |
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for gluco |
1.49 KB |
2015-11-27 |
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9 |
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5 |
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| PubMed |
10466420 |
Homozygosity for a novel DTDST mutation in a child with a 'broad bone-platyspondylic' variant of dia |
756 Bytes |
2015-11-15 |
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18 |
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5 |
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| PubMed |
1676565 |
Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anon |
706 Bytes |
2015-11-23 |
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10 |
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4 |
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