(Q50305690)

2 March 2018

title

A girl with pervasive developmental disorder and complex chromosome rearrangement involving 8p and 10p. (English)

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2 March 2018

pervasive developmental disorder

main subject

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author

Lyn Sonnenberg

2

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2 March 2018

author name string

L Zwaigenbaum

1

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2 March 2018

T Heshka

3

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2 March 2018

S Eastwood

4

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2 March 2018

J Xu

5

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2 March 2018

language of work or name

English

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publication date

1 June 2005

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2 March 2018

Journal of Autism and Developmental Disorders

published in

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2 March 2018

volume

35

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2 March 2018

issue

3

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2 March 2018

page(s)

393-399

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2 March 2018

https://scigraph.springernature.com/pub.10.1007/s10803-005-3307-0

exact match

0 references

cites work

Cloning and characterization of a novel human leptin receptor overlapping transcript-like 1 gene (LEPROTL1).

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10803-005-3307-0

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

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12 December 2020

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12 December 2020

Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families

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12 December 2020

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

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12 December 2020

The human dihydropyrimidinase-related protein 2 gene on chromosome 8p21 is associated with paranoid-type schizophrenia.

1 reference

12 December 2020

Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.

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12 December 2020

FGF-20, a novel neurotrophic factor, preferentially expressed in the substantia nigra pars compacta of rat brain

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12 December 2020

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

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12 December 2020

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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12 December 2020

Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.

1 reference

12 December 2020

Autism: the phenotype in relatives.

1 reference

12 December 2020

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype

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12 December 2020

A genomewide screen for autism susceptibility loci

1 reference

12 December 2020

Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.

1 reference

12 December 2020

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

1 reference

12 December 2020

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

12 December 2020

An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.

1 reference

12 December 2020

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

1 reference

12 December 2020

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

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12 December 2020

An autosomal genomic screen for autism. Collaborative linkage study of autism

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Molecular cloning and genomic structure of human frizzled-3 at chromosome 8p21

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Hereditary spherocytic anemia with deletion of the short arm of chromosome 8.

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12 December 2020

Chromosome 7q: where autism meets language disorder?

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12 December 2020

Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1).

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12 December 2020

Three probands with autistic disorder and isodicentric chromosome 15.

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12 December 2020

A genomic screen of autism: evidence for a multilocus etiology

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Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.

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12 December 2020

Chromosomal abnormalities in a series of children with autistic disorder.

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12 December 2020

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

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12 December 2020

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

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12 December 2020

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).

1 reference

12 December 2020

The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.

1 reference

12 December 2020

Vulnerability markers in the schizophrenia spectrum: implications for phenomenology, genetics, and the identification of the schizophrenia prodrome

1 reference

12 December 2020

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder

1 reference

12 December 2020

10.1007/S10803-005-3307-0

Identifiers

DOI

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2 March 2018

PubMed ID

16119480

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2 March 2018