(Q33414679)

26 July 2017

1 reference

27 January 2021

1 reference

Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review (English)

1 reference

26 July 2017

1 reference

inferred from abstract

neuropsychological tests

1 reference

1 November 2020

1 reference

27 January 2021

1 reference

9

Leda Dalprà

1 reference

26 July 2017

2

Nicoletta Villa

1 reference

26 July 2017

1

Renata Nacinovich

1 reference

26 July 2017

5

Monica Bomba

1 reference

26 July 2017

10

Francesca Neri

1 reference

26 July 2017

4

Fiorenza Broggi

1 reference

26 July 2017

3

Serena Redaelli

1 reference

26 July 2017

7

Agnese Scatigno

1 reference

26 July 2017

8

Angelo Selicorni

1 reference

26 July 2017

6

Patrizia Stoppa

1 reference

26 July 2017

17 April 2014

4 references

26 July 2017

22 April 2019

1 November 2020

27 January 2021

4 references

26 July 2017

22 April 2019

1 November 2020

27 January 2021

7

1 reference

26 July 2017

248

1 reference

Creative Commons Attribution 2.0 Generic

26 July 2017

3 references

22 April 2019

1 November 2020

https://scigraph.springernature.com/pub.10.1186/1756-0500-7-248

27 January 2021

0 references

0 references

cites work

Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

De novo deletion of chromosome 11q13.4-q14.3 in a boy with microcephaly, ptosis and developmental delay

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Interstitial deletion 11q. Case report and review of the literature.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Partial deletion of the long arm of chromosome 11: ten Japanese children.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

21 June 2018

Deletion (11)(q14.1q21).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Interstitial deletion of the long arm of chromosome 11.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Interstitial deletion of 11q.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

An emerging phenotype of proximal 11q deletions.

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1756-0500-7-248

Pseudoachondroplasia with de novo deletion [del(11)(q21q22.2)].

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1756-0500-7-248

A novel case of bilateral high myopia, cataract, and total retinal detachment associated with interstitial 11q deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1756-0500-7-248

Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1756-0500-7-248

Association of polycystic ovary syndrome with an interstitial deletion of the long arm of chromosome 11 [del(11)(q21q23.1)]

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1756-0500-7-248

Familial deletion 11q14.3-q22.1 without apparent phenotypic consequences: a haplosufficient 8.5 Mb region

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4108053

Interstitial deletion of the long arm of one 11 chromosome

31 October 2018

1 reference

12 December 2020

Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3-->q21

1 reference

12 December 2020

Interstitial deletion of the long arm of chromosome 11

1 reference

12 December 2020

Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling

1 reference

12 December 2020

Identifiers

DOI

10.1186/1756-0500-7-248

1 reference

PubMed ID

24742288

Dimensions Publication ID

26 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1756-0500-7-248

9 September 2019

1 reference

26 July 2017

1 reference

PubMed ID

24742288