(Q37564857)

English

Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature

scientific article published on January 2009

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

1 reference

Europe PubMed Central

Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

mosaic trisomy 20

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Z Powis

1

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

R P Erickson

2

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

publication date

1 January 2009

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Journal of Applied Genetics

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

50

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

293-296

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

https://scigraph.springernature.com/pub.10.1007/bf03195686

0 references

A revisit of trisomy 20 mosaicism in prenatal diagnosis--an overview of 103 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal UPD 20 in a hyperactive child with severe growth retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of trisomy 20 by chorionic villus sampling (CVS): a case report with long-term outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatally detected trisomy 20 mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of mosaic trisomy 20 in New Zealand.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinting in Albright's hereditary osteodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long term follow-up of developmental delay in a child with prenatally-diagnosed trisomy 20 mosaicism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic trisomy 20: considerations for genetic counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanding the phenotype of mosaic trisomy 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19638687

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03195686

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

release_25io7vlh7fgzhcnwor6oebntoa

1 reference

https://api.fatcat.wiki/v0/release/25io7vlh7fgzhcnwor6oebntoa

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

ResearchGate publication ID

0 references

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