(Q24322948)

GOA release 2020-03-11

mesoderm development

1 reference

GOA release 2020-03-11

author name string

S Kobayashi

1

0 references

T Kohda

2

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N Miyoshi

3

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Y Kuroiwa

4

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K Aisaka

5

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O Tsutsumi

6

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T Kaneko-Ishino

7

0 references

F Ishino

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

8

0 references

language of work or name

English

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publication date

May 1997

0 references

published in

Human Molecular Genetics

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volume

6

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issue

5

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page(s)

781-6

0 references

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Genomic imprinting and genetic disorders in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Parental imprinting of the mouse insulin-like growth factor II gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

A genetic linkage map of the mouse: current applications and future prospects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Genomic imprinting and chromosomal localization of the human MEST gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Mosaic and polymorphic imprinting of the WT1 gene in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

The 1993-94 Généthon human genetic linkage map

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Experimental embryological analysis of genetic imprinting in mouse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Three-generation dominant transmission of the Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Reevaluation of Russell-Silver syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

Second observation of Silver-Russel syndrome in a carrier of a reciprocal translocation with one breakpoint at site 17q25

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021

The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021

Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021

Phenotypic and genetic analysis of the Silver-Russell syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021

X-linked short stature with skin pigmentation: evidence for heterogeneity of the Russell-Silver syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.5.781

7 January 2021