Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders. (Q37419604)

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23 January 2020

title

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders (English)

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23 January 2020

0 references

18

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23 January 2020

author name string

S Ben-Shachar

1

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23 January 2020

B Lanpher

2

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23 January 2020

J R German

3

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23 January 2020

M Qasaymeh

4

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L Potocki

5

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S C Sreenath Nagamani

6

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L M Franco

7

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23 January 2020

A Malphrus

8

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G W Bottenfield

9

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J E Spence

10

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S Amato

11

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J A Rousseau

12

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B Moghaddam

13

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C Skinner

14

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S A Skinner

15

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S Bernes

16

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N Armstrong

17

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P Stankiewicz

19

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A Patel

20

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S-W Cheung

21

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J R Lupski

22

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A L Beaudet

23

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T Sahoo

24

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23 January 2020

language of work or name

English

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publication date

15 March 2009

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Journal of Medical Genetics

23 January 2020

published in

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23 January 2020

volume

46

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23 January 2020

issue

6

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23 January 2020

page(s)

382-388

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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

23 January 2020

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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

23 August 2017

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Structural variation of chromosomes in autism spectrum disorder

23 August 2017

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Association between microdeletion and microduplication at 16p11.2 and autism

23 August 2017

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22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome

23 August 2017

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Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes

23 August 2017

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Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation

23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19289393

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19289393

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19289393

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2008.064378

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19289393 AND SRC:MED&resulttype=core&format=json

23 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19289393 AND SRC:MED&resulttype=core&format=json

23 January 2020

PubMed publication ID

19289393

1 reference