(Q33881293)

29 July 2017

title

Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome (English)

1 reference

29 July 2017

0 references

Frank J Probst

1

1 reference

29 July 2017

Mitchell Lance Cooper

series ordinal

2

1 reference

29 July 2017

Sau Wai Cheung

series ordinal

3

1 reference

29 July 2017

Monica J Justice

series ordinal

4

1 reference

29 July 2017

publication date

21 May 2008

1 reference

29 July 2017

1 reference

29 July 2017

volume

99

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29 July 2017

issue

5

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29 July 2017

page(s)

512-517

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THE Y-CHROMOSOME AS THE BEARER OF MALE DETERMINING FACTORS IN THE MOUSE

29 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=2877559

EXCEPTIONAL INHERITANCE OF A SEX-LINKED GENE IN THE MOUSE EXPLAINED ON THE BASIS THAT THE X/O SEX-CHROMOSOME CONSTITUTION IS FEMALE

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's 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=2877559

Functional genetic analysis of mouse chromosome 11

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

The human genome browser at UCSC

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

Primer3 on the WWW for general users and for biologist programmers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

Typing of X chromosomes bearing Tabby allele in mouse preimplantation embryos by detection of a microsatellite marker.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

Genes and genotypes affecting the teeth of the mouse

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

The glandular aspects of the tabby syndrome in the mouse

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

28 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FJHERED%2FESN027

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJHERED%2FESN027

A totally sex-linked gene in the house mouse.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877559

Classic pages in obstetrics and gynecology by Henry H. Turner. A syndrome of infantilism, congenital webbed neck, and cubitus valgus. Endocrinology, vol. 23, pp. 566-574, 1938

29 October 2018

1 reference

12 December 2020

The XO and Oy chromosome constitutions in the mouse

1 reference

12 December 2020

Cytogenetic analysis of oocytes and early preimplantation embryos from XO mice

1 reference

12 December 2020

Retarded development of XO conceptuses during early pregnancy in the mouse

1 reference

12 December 2020

Non-Random Segregation during Mammalian Oogenesis

1 reference

12 December 2020

Identifiers

DOI

10.1093/JHERED/ESN027

1 reference

29 July 2017

1 reference

29 July 2017

1 reference