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# proj.
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# Ann.
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updated_at |
| PubMed |
10788334 |
Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer.
We have undertake |
1.53 KB |
2015-11-15 |
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35 |
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24 |
2021-12-05
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| PubMed |
1353340 |
Late-onset metachromatic leukodystrophy: molecular pathology in two siblings.
We report on a new all |
716 Bytes |
2015-11-18 |
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42 |
|
15 |
2021-12-05
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| PubMed |
9294109 |
Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal |
1.33 KB |
2015-12-08 |
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41 |
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27 |
2021-12-05
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| PubMed |
2491010 |
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the |
1.55 KB |
2016-01-17 |
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33 |
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21 |
2021-12-05
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| PubMed |
7668252 |
Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its |
1.43 KB |
2015-03-12 |
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30 |
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24 |
2021-12-05
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| PubMed |
1671881 |
Two distinct mutations at a single BamHI site in phenylketonuria.
Classical phenylketonuria is an au |
701 Bytes |
2015-11-23 |
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33 |
|
10 |
2021-12-05
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| PubMed |
8755918 |
Mutations associated with variant phenotypes in ataxia-telangiectasia.
We have identified 14 familie |
1.31 KB |
2015-11-27 |
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33 |
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15 |
2021-12-05
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| PubMed |
2422478 |
Midline B3 serotonin nerves in rat medulla are involved in hypotensive effect of methyldopa.
Previou |
1.64 KB |
2016-01-15 |
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25 |
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30 |
2021-12-05
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| PubMed |
1848636 |
Debrisoquine phenotype and the pharmacokinetics and beta-2 receptor pharmacodynamics of metoprolol a |
1.78 KB |
2015-12-07 |
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25 |
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29 |
2021-12-05
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| PubMed |
19048115 |
Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and co-occur with TP53 m |
1.67 KB |
2015-11-24 |
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28 |
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41 |
2021-12-05
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