A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 35, doi. 10.1007/s10048-008-0143-3
- By:
- Publication type:
- Article
Works matching IS 13646745 AND DT 2009 AND VI 10 AND IP 1
Results: 13
1
2
Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 43, doi. 10.1007/s10048-008-0144-2
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- Publication type:
- Article
3
Molecular and functional analysis of the HEXB gene in Italian patients affected with Sandhoff disease: identification of six novel alleles.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 49, doi. 10.1007/s10048-008-0145-1
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- Publication type:
- Article
4
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9–2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP).
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 59, doi. 10.1007/s10048-008-0148-y
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- Publication type:
- Article
5
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 65, doi. 10.1007/s10048-008-0149-x
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- Publication type:
- Article
6
Alzheimer’s disease risk variants show association with cerebrospinal fluid amyloid beta.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 13, doi. 10.1007/s10048-008-0150-4
- By:
- Publication type:
- Article
7
Assessment of Alzheimer’s disease case–control associations using family-based methods.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 19, doi. 10.1007/s10048-008-0151-3
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- Publication type:
- Article
8
MS and autoimmune disorders.
- Published in:
- 2009
- By:
- Publication type:
- Editorial
9
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 73, doi. 10.1007/s10048-008-0153-1
- By:
- Publication type:
- Article
10
Expression analysis of genes lying in the NF1 microdeletion interval points to four candidate modifiers for neurofibroma formation.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 79, doi. 10.1007/s10048-008-0154-0
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- Publication type:
- Article
11
Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 27, doi. 10.1007/s10048-008-0155-z
- By:
- Publication type:
- Article
12
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 5, doi. 10.1007/s10048-008-0156-y
- By:
- Publication type:
- Article
13
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
- Published in:
- 2009
- By:
- Publication type:
- Correction Notice