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source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| PubMed |
11773892 |
End-stage renal disease (ESRD) after orthotopic liver transplantation (OLTX) using calcineurin-based |
2.71 KB |
2015-11-21 |
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23 |
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33 |
2021-12-22
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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 |
|
6 |
2021-12-22
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| PubMed |
14722929 |
Low frequency of deafness-associated GJB2 variants in Kenya and Sudan and novel GJB2 variants.
A lar |
1.71 KB |
2015-11-22 |
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25 |
|
6 |
2021-12-22
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| PubMed |
15000256 |
Single-strand conformation polymorphism analysis of the FMR1 gene in autistic and mentally retarded |
1.15 KB |
2015-11-18 |
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26 |
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6 |
2021-12-22
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| PubMed |
15033202 |
Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
The Nijme |
2.03 KB |
2015-11-18 |
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25 |
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20 |
2021-12-22
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| PubMed |
15042318 |
Atrial fibrillation following chemotherapy for stage IIIE diffuse large B-cell gastric lymphoma in a |
725 Bytes |
2017-09-04 |
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25 |
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12 |
2021-12-22
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| PubMed |
15069170 |
Four novel mutations in the thiazide-sensitive Na-Cl co-transporter gene in Japanese patients with G |
1.81 KB |
2015-11-22 |
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25 |
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9 |
2021-12-22
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| PubMed |
15086325 |
Identification of three F5 gene mutations associated with inherited coagulation factor V deficiency |
1.38 KB |
2015-11-22 |
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24 |
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1 |
2021-12-22
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| PubMed |
15111599 |
CRYBA3/A1 gene mutation associated with suture-sparing autosomal dominant congenital nuclear catarac |
1.57 KB |
2015-11-22 |
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24 |
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6 |
2021-12-22
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| PubMed |
15130900 |
Urinary bladder cancer in Wegener's granulomatosis: risks and relation to cyclophosphamide.
OBJECTIV |
1.77 KB |
2021-11-28 |
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23 |
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19 |
2021-12-22
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