Familial 2/3 translocation (Q35231288)

7 August 2017

title

Familial 2/3 translocation. (English)

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7 August 2017

Summitt RL

1

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7 August 2017

language of work or name

English

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publication date

1 March 1966

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

18

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7 August 2017

issue

2

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7 August 2017

page(s)

172-186

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Familial Mongolism (Trisomy-21 Syndrome) Resulting from a "15/21" Chromosome Translocation in More than Three Generations of a Large Kindred.

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706162

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706162

Dermal patterns of 18 and D1 trisomics

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706162

Chromosome preparations of leukocytes cultured from human peripheral blood

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706162

Partial-trisomy syndromes. I. Sturge-Weber's disease.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706162

Chromosomal translocations in patients with mongolism and in their normal relatives.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706162

PARTIAL TRISOMY-DEFICIENCY SYNDROME RESULTING FROM A RECIPROCAL TRANSLOCATION IN A LARGE KINDRED

26 September 2018

1 reference

12 December 2020

Familial translocation mongolism: a carrier exhibiting nonacrocentric translocation

1 reference

12 December 2020

PRESUMED TRANSLOCATION OF CHROMOSOME NUMBER 2 AND ONE OF THE D GROUP

1 reference

12 December 2020

Normal arotype/translocation mosaic

1 reference

12 December 2020

A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES

1 reference

12 December 2020

Chromosome translocation as a cause of familial mongolism

1 reference

12 December 2020

FAMILIAL 2 - 22 TRANSLOCATION; ASSOCIATION WITH A HAPLO-X TURNER'S SYNDROME

1 reference

12 December 2020

FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"

1 reference

12 December 2020

PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18

1 reference

12 December 2020

PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE

1 reference

12 December 2020

1 reference

12 December 2020

Chromosomal abnormalities in father and Mongol child

1 reference

12 December 2020

A Mongol girl with 46 chromosomes

1 reference

12 December 2020

Familial Langdon Down anomaly with chromosomal fusion

1 reference

12 December 2020

Identifiers

PMC publication ID

1706162

1 reference

7 August 2017

1 reference