22q11 deletion syndrome in adults with schizophrenia (Q35214115)

7 August 2017

title

22q11 deletion syndrome in adults with schizophrenia (English)

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7 August 2017

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22q11 deletion syndrome

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A S Bassett

1

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7 August 2017

K Hodgkinson

2

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7 August 2017

E W Chow

3

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7 August 2017

S Correia

4

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7 August 2017

L E Scutt

5

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7 August 2017

R Weksberg

6

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7 August 2017

publication date

1 July 1998

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American Journal of Medical Genetics Part A

7 August 2017

published in

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7 August 2017

volume

81

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7 August 2017

issue

4

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7 August 2017

page(s)

328-337

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

7 August 2017

cites work

1 reference

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28 July 2018

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Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician

28 July 2018

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Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

28 July 2018

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Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?

28 July 2018

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Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome

28 July 2018

1 reference

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Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations

28 July 2018

1 reference

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Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

28 July 2018

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Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature

28 July 2018

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Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome

28 July 2018

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On the plausibility of "the neurodevelopmental hypothesis" of schizophrenia

28 July 2018

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Prevalence of 22q11 microdeletion

28 July 2018

1 reference

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A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

28 July 2018

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How many breaks do we need to CATCH on 22q11?

28 July 2018

1 reference

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

28 July 2018

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DiGeorge syndrome: part of CATCH 22.

28 July 2018

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Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

28 July 2018

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28 July 2018

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Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics

28 July 2018

1 reference

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Child development risk factors for adult schizophrenia in the British 1946 birth cohort

28 July 2018

1 reference

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Childhood antecedents of schizophrenia and affective illness: social adjustment at ages 7 and 11

28 July 2018

1 reference

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Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

28 July 2018

1 reference

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Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions

28 July 2018

1 reference

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Schizophrenia: genetic tools for unraveling the nature of a complex disorder

28 July 2018

1 reference

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DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.

28 July 2018

1 reference

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The velo-cardio-facial syndrome: a clinical and genetic analysis

28 July 2018

1 reference

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Velo-cardio-facial syndrome: language and psychological profiles.

28 July 2018

1 reference

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Anomalies associated with cleft lip, cleft palate, or both

28 July 2018

1 reference

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Is schizophrenia a neurodevelopmental disorder?

28 July 2018

1 reference

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Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise

28 July 2018

1 reference

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A cognitive and behavioural phenotype in williams syndrome

28 July 2018

1 reference

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Centiles for adult head circumference

28 July 2018

1 reference

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Chromosomal aberrations and schizophrenia. Autosomes

28 July 2018

1 reference

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Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

28 July 2018

1 reference

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A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Genetic basis of schizophrenia

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Cerebellar atrophy in a patient with velocardiofacial syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Epidemiology of Schizophrenia

24 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173497

Schizophrenia and the myth of intellectual decline

8 December 2018

1 reference

12 December 2020

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

12 December 2020

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

1 reference

12 December 2020

Duration of psychosis and outcome in first-episode schizophrenia

1 reference

12 December 2020

The otolaryngologist and the patient with velocardiofacial syndrome

1 reference

12 December 2020

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

12 December 2020

Velocardiofacial syndrome: analysis of phoniatric and other clinical findings

1 reference

12 December 2020

Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2.

1 reference

12 December 2020

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study

1 reference

12 December 2020

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion

1 reference

12 December 2020

Schizophrenia, CATCH 22 and FISH

1 reference

12 December 2020

The search for hemizygosity at 22qll in patients with isolated cleft palate

1 reference

12 December 2020

10.1002/(SICI)1096-8628(19980710)81:4<328::AID-AJMG10>3.3.CO;2-8

Identifiers

DOI

1 reference

7 August 2017

1 reference

7 August 2017

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