Found: 7
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Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.
- Published in:
- Molecular Psychiatry, 2012, v. 17, n. 12, p. 1328, doi. 10.1038/mp.2011.129
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- Publication type:
- Article
The Gitelman syndrome mutation, IVS9+1G>T, is common across Europe.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Cystic fibrosis patients from the black sea region: The 1677delTA mutation.
- Published in:
- Human Mutation, 1994, v. 3, n. 4, p. 353, doi. 10.1002/humu.1380030405
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- Publication type:
- Article
Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 1, p. 82, doi. 10.1111/j.1399-0004.2008.01024.x
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- Publication type:
- Article
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
- Published in:
- 1999
- By:
- Publication type:
- journal article
A chromosome 10p11.2 GT-dinucleotide repeat polymorphism at the GLUDP5 gene locus.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1328
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- Publication type:
- Article