(Q50313091)

2 March 2018

title

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype. (English)

1 reference

2 March 2018

main subject

22q13 deletion syndrome

1 reference

1 reference

Prasad C

1

1 reference

2 March 2018

Prasad AN

2

1 reference

2 March 2018

Chodirker BN

3

1 reference

2 March 2018

Lee C

4

1 reference

2 March 2018

Dawson AK

5

1 reference

2 March 2018

Jocelyn LJ

6

1 reference

2 March 2018

Chudley AE

7

1 reference

2 March 2018

publication date

1 February 2000

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2 March 2018

published in

Clinical Genetics

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2 March 2018

volume

57

1 reference

2 March 2018

page(s)

103-109

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2 March 2018

issue

2

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2 March 2018

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Outcomes of genetic evaluation in children with pervasive developmental disorder.

21 January 2018

1 reference

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Children with PDD need to be evaluated by clinical geneticists. Pervasive developmental disorder.

21 January 2018

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The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

21 January 2018

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Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome

21 January 2018

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21 January 2018

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Brief report: cognitive and behavioral profiles in persons with Smith-Magenis syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Terminal 22q deletion associated with a partial deficiency of arylsulphatase A

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Deletion mapping by FISH with BACs in patients with partial monosomy 22q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Two 22q telomere deletions serendipitously detected by FISH

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Characterization of a human gene related to genes encoding somatostatin receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

Cytoarchitectonic anomalies in a genetically based disorder: Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570203.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2000.570203.X

1 reference

2 March 2018

PubMed ID

10735630

1 reference

2 March 2018