Maternal origin of inv dup(15) chromosomes in infantile autism (Q50302844)

From Wikidata

Jump to navigation Jump to search

scientific article published in December 1996

edit

Language	Label	Description	Also known as
English	Maternal origin of inv dup(15) chromosomes in infantile autism	scientific article published in December 1996

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

title

Maternal origin of inv dup(15) chromosomes in infantile autism (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

main subject

autism

0 references

author

Tommy Martinsson

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

Christopher Gillberg

series ordinal

6

object named as

C Gillberg

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

author name string

T Johannesson

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

M Vujic

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

A Sjöstedt

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

S Steffenburg

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

J Wahlström

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

publication date

1 December 1996

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

published in

European Child & Adolescent Psychiatry

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

volume

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

page(s)

185-192

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

cites work

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism in Angelman syndrome: a population-based study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism associated with marker chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a marker chromosome as inv dup(15) by molecular analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic and clinical studies in five cases of inv dup(15)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication error, a new hypothesis to explain the origin of a supernumerary marker chromosome in a mentally retarded boy.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Emanuel Miller Memorial Lecture 1991. Autism and autistic-like conditions: subclasses among disorders of empathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal insertion of human papillomavirus 18 sequences in HeLa cells detected by nonisotopic in situ hybridization and reflection contrast microscopy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of chromosome 18 in a girl with mental retardation and autistic disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential maternal derivation in inv dup(15): analysis of eight new cases.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome findings in twins with early-onset autistic disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular study of the Prader-Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved technique for chromosome preparations from human lymphocytes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the GABAA receptor beta 3 (GABRB3) locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental paternal disomy in Angelman's syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of autism associated with partial tetrasomy 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8989557

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00538845

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

PubMed publication ID

8989557

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8989557

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/8989557

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50302844&oldid=2247974296"