(Q50308230)

English

Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.

scientific article published on 13 May 2004

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scholarly article

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy. (English)

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

intractable epilepsy

1 reference

based on heuristic

inferred from title

author name string

S M Mann

1

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

N J Wang

2

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

D H Liu

3

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

L Wang

4

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

R A Schultz

5

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

N Dorrani

6

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

M Sigman

7

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

N C Schanen

8

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

publication date

13 May 2004

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

115

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Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

104-111

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

2

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

https://scigraph.springernature.com/pub.10.1007/s00439-004-1127-5

0 references

Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial hexasomy of chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Settings as an important dimension in health education/promotion policy, programs, and research.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimate of the prevalence of chromosome 15q11-q13 duplications

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unusual tricentric X chromosome detected prenatally

1 reference

https://pubmed.ncbi.nlm.nih.gov/15141347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-004-1127-5

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

1 reference

Europe PubMed Central

2 March 2018

http://europepmc.org/abstract/MED/15141347

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