(Q33678597)

English

Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child

scientific article

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child (English)

1 reference

Europe PubMed Central

28 July 2017

0 references

author name string

Dean J

1

1 reference

Europe PubMed Central

28 July 2017

Cohen G

2

1 reference

Europe PubMed Central

28 July 2017

Kemp J

3

1 reference

Europe PubMed Central

28 July 2017

Robson L

4

1 reference

Europe PubMed Central

28 July 2017

Tembe V

5

1 reference

Europe PubMed Central

28 July 2017

Hasselaar J

6

1 reference

Europe PubMed Central

28 July 2017

Webster B

7

1 reference

Europe PubMed Central

28 July 2017

Lammi A

8

1 reference

Europe PubMed Central

28 July 2017

Smith A

9

1 reference

Europe PubMed Central

28 July 2017

language of work or name

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publication date

1 March 1997

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

28 July 2017

34

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Europe PubMed Central

28 July 2017

3

1 reference

Europe PubMed Central

28 July 2017

246-249

1 reference

Europe PubMed Central

28 July 2017

A case of full triploidy (69,XXX) of paternal origin with unusually long survival time

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Chimaerism shown by cytogenetics and DNA polymorphism analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Chromosomal mosaicism confined to the placenta in human conceptions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

46,X,i(Xq)/47,XX,+13 mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Tissue-specific 45,X0/47,XY,+13 mosaicism in an 18-year-old woman

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Mean red cell volume in normal, anemic, small, trisomic and triploid fetuses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Mosaic trisomy 16 in a live newborn infant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Turner/Down mosaicism. A case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Mosaic 45,x/47,xy,+18.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050902

21 June 2018

Double mosaic aneuploidy: 45,X/47,XY,+8 in a male infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up of case of advanced survival and trisomy 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association between fetal karyotype and mean corpuscular volume

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A specific phenotype associated with trisomy 15 mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.34.3.246

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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