(Q34674854)

3 August 2017

1 reference

title

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism (English)

1 reference

3 August 2017

Thomas IT

1

1 reference

3 August 2017

Frias JL

2

1 reference

3 August 2017

Cantu ES

3

1 reference

3 August 2017

Lafer CZ

4

1 reference

3 August 2017

Flannery DB

5

1 reference

3 August 2017

Graham JG Jr

6

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 August 1989

1 reference

American Journal of Human Genetics

3 August 2017

1 reference

3 August 2017

45

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3 August 2017

2

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3 August 2017

193-205

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GENERALIZED UNBALANCED MOSAICISM ATTRIBUTABLE TO DISPERMY AND PROBABLE FERTILIZATION OF A POLAR BODY

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Gene action in the X-chromosome of the mouse (Mus musculus L.)

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Ring chromosome 14: a distinct clinical entity

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Aberrant melanoblast migration associated with trisomy 18 mosaicism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

A boy with ring chromosome 15 derived from a t(15q;15q) robertsonian translocation in the mother: Cytogenetic and biochemical findings

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

A case of XX/XY mosaicism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

A human ring D chromosome associated with multiple congenital abnormalities

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Ring chromosomes in two infants with congenital malformations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Gene control of mammalian pigmentary differentiation. I. Clonal origin of melanocytes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Tetraploidy and 18-trisomy in a six-year-old triple mosaic boy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Lyonization and the lines of Blaschko

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

A true hermaphrodite dispermic chimera with 46,XX and 46,XY karyotypes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Trisomy 14 mosaicism: case report and review

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Ocular Findings in Triploidy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

CONGENITAL ASYMMETRY ASSOCIATED WITH DIPLOID-TRIPLOID MOSAICISM AND LARGE SATELLITES

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683341

The pallister mosaic syndrome

26 October 2018

1 reference

12 December 2020

Pigment anomalies of the skin in the human chimaera: their relation to systematized naevi

1 reference

12 December 2020

Diploid-triploid mosaicism: delineation of the syndrome

1 reference

12 December 2020

Cytogenetics of ring chromosome 7

1 reference

12 December 2020

Teschler-Nicola/Killian syndrome: a case report

1 reference

12 December 2020

Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata

1 reference

12 December 2020

Diploid/triploid mixoploidy and hypomelanosis of Ito

1 reference

12 December 2020

Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases

1 reference

12 December 2020

Identifiers

PMCID

1683341

1 reference

3 August 2017

1 reference