(Q35148451)

6 August 2017

1 reference

title

Mutational risks in females: genomic imprinting and maternal molecules (English)

1 reference

6 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1279402

8 September 2022

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

20 November 2023

author name string

G. N. Wilson

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1279402

8 September 2022

language of work or name

English

0 references

publication date

1 December 1992

1 reference

full work available at URL

6 August 2017

https://api.elsevier.com/content/article/PII:016511109290039C?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

https://api.elsevier.com/content/article/PII:016511109290039C?httpAccept=text/plain

20 November 2023

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

20 November 2023

1 reference

6 August 2017

volume

296

1 reference

6 August 2017

issue

1-2

1 reference

6 August 2017

page(s)

157-165

1 reference

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

6 August 2017

cites work

2

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Molecular biology of the sea urchin embryo.

20 November 2023

4

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene

20 November 2023

7

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Mutagen-induced fetal anomalies and death following treatment of females within hours after mating

20 November 2023

8

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

X linked mental retardation

20 November 2023

9

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

20 November 2023

10

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

20 November 2023

Genomic imprinting

12

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

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

20 November 2023

13

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Vegetal messenger RNA localization directed by a 340-nt RNA sequence element in Xenopus oocytes

20 November 2023

15

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

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

20 November 2023

16

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Genomic imprinting and embryonal tumours

20 November 2023

17

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Oct-3 and the beginning of mammalian development

20 November 2023

18

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

The paternal genome in mouse zygotes is less sensitive to ENU mutagenesis than the maternal genome.

20 November 2023

19

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

High frequency of mosaic mutants produced by N-ethyl-N-nitrosourea exposure of mouse zygotes

20 November 2023

20

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Frequency and nature of specific-locus mutations induced in female mice by radiations and chemicals: a review

20 November 2023

21

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Complementation studies with mouse translocations

20 November 2023

22

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Differential imprinting and expression of maternal and paternal genomes

20 November 2023

23

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Uniparental disomy as a mechanism for human genetic disease

20 November 2023

24

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Transgenes as molecular probes for genomic imprinting.

20 November 2023

25

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

20 November 2023

Mutation in man

26

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

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

20 November 2023

27

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

Balanced translocation 12/13 and situs abnormalities: homology of early pattern formation in man and lower organisms?

20 November 2023

30

1 reference

https://api.crossref.org/works/10.1016/0165-1110(92)90039-C

20 November 2023

Identifiers

1 reference

6 August 2017

1 reference