(Q34192686)

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Genomic imprinting

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scholarly article

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Europe PubMed Central

Genomic imprinting (English)

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Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Hall JG

1

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Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

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publication date

1 October 1990

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Europe PubMed Central

PubMed publication ID

31 July 2017

Archives of Disease in Childhood

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Europe PubMed Central

PubMed publication ID

31 July 2017

65

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Europe PubMed Central

PubMed publication ID

31 July 2017

10 Spec No

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1013-1015

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Differential activity of maternally and paternally derived chromosome regions in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Is Angelman syndrome an alternate result of del(15)(q11q13)?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Transgenes as molecular probes for genomic imprinting.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Differential imprinting and expression of maternal and paternal genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Uniparental disomy as a mechanism for human genetic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Chromosome maps of man and mouse. IV.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Genome imprinting and dominance modification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1590263

5 July 2018

Factors affecting the observed number of young resulting from adjacent-2 disjunction in mice carrying a translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2241218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/ADC.65.10_SPEC_NO.1013

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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