(Q28218867)

2

0 references

Alfried Kohlschütter

object named as

Alfried Kohlschütter

7

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Graziella Uziel

5

object named as

Graziella Uziel

0 references

Thomas Bettecken

10

object named as

Thomas Bettecken

0 references

author name string

Claudia Rubie

1

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Jutta Gärtner

3

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Markus Siekiera

4

0 references

Bernd Kohlmann

6

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Gerald Stöber

22q11 deletion syndrome: a genetic subtype of schizophrenia

9

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language of work or name

English

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publication date

January 2003

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published in

Human Mutation

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volume

21

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issue

1

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page(s)

45-52

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cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Genetic heterogeneity in catatonic schizophrenia: a family study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Structural models of the transmembrane region of voltage-gated and other K+ channels in open, closed, and inactivated conformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Linkage and associated studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Megalencephaly and leukodystrophy with mild clinical course: a report on 12 new cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtel

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical course.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Polymorphic markers for the arylsulfatase A gene reveal a greatly expanded meiotic map for the human 22q telomeric region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

Recent advances in the neuropathology of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Molecular genetics of metachromatic leukodystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Velo-cardio-facial syndrome: a review of 120 patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Sex identification by polymerase chain reaction using X-Y homologous primer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Periodic catatonia: A schizophrenic subtype with major gene effect and anticipation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and II

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021

Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10145

7 January 2021