Characterization of the human β4 nAChR gene and polymorphisms in CHRNA3 and CHRNB4.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 7, p. 362, doi. 10.1007/PL00010921
- By:
- Publication type:
- Article
Works matching AU Bercovich, D.
Results: 8
1
2
Severe infantile male encephalopathy is a result of early post-zygotic WDR45 somatic mutation.
- Published in:
- Clinical Genetics, 2016, v. 90, n. 6, p. 560, doi. 10.1111/cge.12849
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- Publication type:
- Article
3
A Mutation Analysis of the Phenylalanine Hydroxylase ( PAH) Gene in the Israeli Population.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 3, p. 305, doi. 10.1111/j.1469-1809.2007.00425.x
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- Publication type:
- Article
4
Familial adenomatous polyposis.
- Published in:
- 2009
- By:
- Publication type:
- journal article
5
SFB-based S-haplotyping of apricot ( Prunus armeniaca) with DHPLC.
- Published in:
- Plant Breeding, 2009, v. 128, n. 6, p. 707, doi. 10.1111/j.1439-0523.2008.01613.x
- By:
- Publication type:
- Article
6
The Two-Brains Hypothesis: Towards a guide for brain-brain and brain-machine interfaces.
- Published in:
- Journal of Integrative Neuroscience, 2015, v. 14, n. 3, p. 281, doi. 10.1142/S0219635215500235
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- Publication type:
- Article
7
Electromagnetic induction between axons and their Schwann cell myelin-protein sheaths.
- Published in:
- Journal of Integrative Neuroscience, 2013, v. 12, n. 4, p. 475, doi. 10.1142/S0219635213500295
- By:
- Publication type:
- Article
8
RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations.
- Published in:
- British Journal of Dermatology, 2008, v. 158, n. 5, p. 1035, doi. 10.1111/j.1365-2133.2008.08493.x
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- Publication type:
- Article