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source ID
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# proj.
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# Ann.
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updated_at |
| PubMed |
9385378 |
A novel common missense mutation G301C in the N-acetylgalactosamine-6-sulfate sulfatase gene in muco |
1.29 KB |
2015-11-27 |
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43 |
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7 |
2025-01-16
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| PubMed |
9391879 |
Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer families.
In this study |
923 Bytes |
2015-11-27 |
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40 |
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5 |
2025-01-16
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| PubMed |
9391889 |
Paternal transmission of congenital myotonic dystrophy.
We report a rare case of paternally transmit |
1.07 KB |
2015-03-12 |
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42 |
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14 |
2025-01-16
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| PubMed |
9400934 |
The RB1 gene mutation in a child with ectopic intracranial retinoblastoma.
The RB1 gene mutation was |
770 Bytes |
2015-11-28 |
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48 |
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5 |
2025-01-16
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| PubMed |
941901 |
Low levels of beta hexosaminidase A in healthy individuals with apparent deficiency of this enzyme.
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1.19 KB |
2015-12-04 |
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41 |
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8 |
2025-01-16
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| PubMed |
9420335 |
The tumor suppressor gene Smad4/Dpc4 is required for gastrulation and later for anterior development |
1.01 KB |
2015-03-12 |
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40 |
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6 |
2025-01-16
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| PubMed |
9425228 |
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Fa |
1.01 KB |
2015-11-27 |
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41 |
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6 |
2025-01-16
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| PubMed |
9425239 |
Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy pati |
1.5 KB |
2015-11-28 |
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41 |
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7 |
2025-01-16
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| PubMed |
9427148 |
Aspartylglucosaminuria among Palestinian Arabs.
Aspartylglucosaminuria (AGU) is a rare disorder of g |
843 Bytes |
2015-11-27 |
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48 |
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8 |
2025-01-16
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| PubMed |
9439660 |
Detection of heterozygous carriers of the ataxia-telangiectasia (ATM) gene by G2 phase chromosomal r |
1.3 KB |
2015-11-27 |
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41 |
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13 |
2025-01-16
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