Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene (Q33856496)

29 July 2017

title

Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene (English)

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29 July 2017

7

Stephen W Scherer

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Mohammad M Ghahramani Seno

29 July 2017

object named as

Mohammad M Ghahramani Seno

1

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Rainald Moessner

4

object named as

Rainald Moessner

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29 July 2017

Benjamin Y M Kwan

2

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29 July 2017

Ka Ki M Lee-Ng

3

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29 July 2017

Anath C Lionel

5

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29 July 2017

Christian R Marshall

6

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29 July 2017

publication date

26 March 2011

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29 July 2017

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29 July 2017

volume

12

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29 July 2017

page(s)

45

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Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

29 July 2017

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5 July 2018

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Functional impact of global rare copy number variation in autism spectrum disorders

5 July 2018

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Towards a comprehensive structural variation map of an individual human genome

5 July 2018

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The clinical context of copy number variation in the human genome

5 July 2018

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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

5 July 2018

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Large, rare chromosomal deletions associated with severe early-onset obesity

5 July 2018

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Origins and functional impact of copy number variation in the human genome

5 July 2018

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Whole genome scanning: resolving clinical diagnosis and management amidst complex data

5 July 2018

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Structural variation of chromosomes in autism spectrum disorder

5 July 2018

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Male germ cell-specific expression of a novel Patched-domain containing gene Ptchd3

5 July 2018

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5 July 2018

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Germ-line DNA copy number variation frequencies in a large North American population

5 July 2018

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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

5 July 2018

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Global variation in copy number in the human genome

5 July 2018

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5 July 2018

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Gene losses during human origins

5 July 2018

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Structural variation in the human genome

5 July 2018

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Detection of large-scale variation in the human genome

5 July 2018

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Large-scale copy number polymorphism in the human genome

5 July 2018

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A human genome diversity cell line panel

5 July 2018

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When less is more: gene loss as an engine of evolutionary change

5 July 2018

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Hedgehog and its patched-smoothened receptor complex: a novel signalling mechanism at the cell surface

5 July 2018

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Inherited resistance to HIV-1 conferred by an inactivating mutation in CC chemokine receptor 5: studies in populations with contrasting clinical phenotypes, defined racial background, and quantified risk

5 July 2018

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5 July 2018

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Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy–negative individuals

5 July 2018

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Common deletion polymorphisms in the human genome.

5 July 2018

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Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study

21 January 2018

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Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements

21 January 2018

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Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

21 January 2018

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Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?

21 January 2018

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Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease.

21 January 2018

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29 October 2018

Identifiers

DOI

10.1186/1471-2350-12-45

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Dimensions Publication ID

29 July 2017

0 references

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29 July 2017

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