(Q51961478)

English

Maternal uniparental heterodisomy for chromosome 2: detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case.

scientific article published in October 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Maternal uniparental heterodisomy for chromosome 2: detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Judith A Goodship

6

object named as

Goodship JA

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

author name string

Wolstenholme J

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

White I

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Sturgiss S

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Carter J

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Plant N

5

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

publication date

1 October 2001

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Prenatal Diagnosis

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

21

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

10

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

813-817

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

Trisomy 2: confined placental mosaicism in a fetus with intrauterine growth retardation

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Postnatal placental confirmation of trisomy 2 and trisomy 16 detected at chorionic villus sampling: a possible association with intrauterine growth retardation and elevated maternal serum alpha-fetoprotein

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Follow-up of pregnancies complicated by placental mosaicism diagnosed by chorionic villus sampling

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes?

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

The European collaborative study on mosaicism in chorionic villus sampling: data from 1986 to 1987.

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

An audit of trisomy 16 in man.

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Cytogenetic analysis of chorionic villi for prenatal diagnosis: an ACC collaborative study of U.K. data. Association of Clinical Cytogeneticists Working Party on Chorionic Villi in Prenatal Diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Confined placental mosaicism for trisomy 2 with intrauterine growth retardation and severe oligohydramnios in the absence of uniparental disomy in the fetus

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

MATERNAL SERUM SCREENING AND TRISOMY 16 CONFINED TO THE PLACENTA

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Maternal uniparental disomy (UPD) for chromosome 2 discovered by exclusion of paternity

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Cytogenetic results from the U.S. Collaborative Study on CVS

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

A case of mosaic trisomy 2 diagnosed at amniocentesis in an abnormal fetus and confirmed in multiple fetal tissues

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Analysis of nine pregnancies with confined placental mosaicism for trisomy 2

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation

1 reference

https://api.crossref.org/works/10.1002%2FPD.143

21 January 2018

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/11746120

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