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Schizophrenia and genetics: new insights.

Schizophrenia and genetics: new insights.

http://www.wikidata.org/entity/Q34749234

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Disruption of the neurexin 1 gene is associated with schizophrenia Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44.Whether ionizing radiation is a risk factor for schizophrenia spectrum disorders?Association of synapsin 2 with schizophrenia in families of Northern European ancestry Asymmetric crying facies in the 22q11.2 deletion syndrome: implications for future screening.Perioperative risk factors in patients with 22q11.2 deletion syndrome requiring surgery for velopharyngeal dysfunction.Extreme population differences across Neuregulin 1 gene, with implications for association studies.Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis.

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Schizophrenia and genetics: new insights.

http://www.wikidata.org/entity/Q34749234

description

2002 nî lūn-bûn

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2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի օգոստոսին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Schizophrenia and genetics: new insights.

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Current Psychiatry Reports

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Schizophrenia and genetics: new insights.

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Anne S Bassett

http://www.w3.org/2001/XMLSchema#string

Eva W Chow

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Linda Brzustowicz

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Rosanna Weksberg

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P2860

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

A common molecular basis for rearrangement disorders on chromosome 22q11

The DNA sequence of human chromosome 22

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

Confirming unexpressed genotypes for schizophrenia. Risks in the offspring of Fischer's Danish identical and fraternal discordant twins.

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