(Q33678031)

28 July 2017

title

Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22. (English)

1 reference

28 July 2017

Dawson AJ

1

1 reference

28 July 2017

Mears AJ

2

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28 July 2017

Chudley AE

3

1 reference

28 July 2017

Bech-Hansen T

4

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28 July 2017

McDermid H

5

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28 July 2017

language of work or name

English

0 references

publication date

1 November 1996

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

33

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28 July 2017

issue

11

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28 July 2017

page(s)

952-956

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Chromosome preparations of leukocytes cultured from human peripheral blood

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Nondisjunction of chromosome 15: origin and recombination

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Molecular characterization of the marker chromosome associated with cat eye syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

A map of 22 loci on human chromosome 22.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

11Q;22Q translocation: Third case of imbalance not due to 3:1 nondisjunction in first meiosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050791

The 11q;22q translocation: a European collaborative analysis of 43 cases

21 June 2018

1 reference

12 December 2020

Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

1 reference

12 December 2020

Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis

1 reference

12 December 2020

Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3:1 segregation at meiosis I

1 reference

12 December 2020

The translocation 11q;22q: a novel unbalanced karyotype

1 reference

12 December 2020

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid

1 reference

12 December 2020

Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter

1 reference

12 December 2020

Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter

1 reference

12 December 2020

The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.33.11.952

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28 July 2017

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28 July 2017

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