(Q58923918)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1

1 reference

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17 January 2020

Giuseppe Novelli

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

Cristina Peconi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Raffaella Cascella

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Cecilia Sinibaldi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Anna Maria Nardone

5

1 reference

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17 January 2020

publication date

1 December 2008

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17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

29

1 reference

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17 January 2020

issue

23

1 reference

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17 January 2020

page(s)

4775-4779

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

A new genetic concept: uniparental disomy and its potential effect, isodisomy

17 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

A fascination with chromosome rescue in uniparental disomy: Mendelian recessive outlaws and imprinting copyrights infringements

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

On the parental origin of the deletion in Angelman syndrome

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Angelman syndrome: a review of the clinical and genetic aspects

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Paternity Testing Commission of the International Society of Forensic Genetics. Recommendations on genetic investigations in paternity cases.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800047

7 January 2021

Identifiers

DOI

10.1002/ELPS.200800047

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19053076%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference