Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier. (Q35196696)

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9 October 2019

title

Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier (English)

1 reference

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9 October 2019

author name string

Wang JC

1

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9 October 2019

Passage MB

2

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9 October 2019

Yen PH

3

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9 October 2019

Shapiro LJ

4

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9 October 2019

Mohandas TK

5

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9 October 2019

language of work or name

English

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publication date

1 June 1991

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American Journal of Human Genetics

9 October 2019

published in

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9 October 2019

volume

48

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9 October 2019

issue

6

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9 October 2019

page(s)

1069-1074

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

9 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Variable number of tandem repeat (VNTR) markers for human gene mapping

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Isolation and mapping of a polymorphic DNA sequence (pCMM12) on chromosome 1p [D1S76]

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Isolation and mapping of a polymorphic DNA sequence (pCMM66) on chromosome 14 [D14S22]

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Uniparental disomy as a mechanism for human genetic disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Genomic imprinting: review and relevance to human diseases.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

Genomic imprinting determines methylation of parental alleles in transgenic mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683099

The use of intensifying screens or organic scintillators for visualizing radioactive molecules resolved by gel electrophoresis

26 September 2018

1 reference

12 December 2020

Degree of methylation of transgenes is dependent on gamete of origin

1 reference

12 December 2020

Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting

1 reference

12 December 2020

Parental origin effects in mice

1 reference

12 December 2020

Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation.

1 reference

12 December 2020

Identifiers

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9 October 2019

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