Cytogenetic approaches to mouse models of human genetic diseases.

about

Cytogenetic approaches to mouse models of human genetic diseases.

Item

http://www.wikidata.org/entity/Q35863470

description

1980 nî lūn-bûn

@nan

1980年の論文

@ja

1980年論文

@yue

1980年論文

@zh-hant

1980年論文

@zh-hk

1980年論文

@zh-mo

1980年論文

@zh-tw

1980年论文

@wuu

1980年论文

@zh

1980年论文

@zh-cn

name

Cytogenetic approaches to mouse models of human genetic diseases.

@ast

Cytogenetic approaches to mouse models of human genetic diseases.

@en

type

Item

label

Cytogenetic approaches to mouse models of human genetic diseases.

@ast

Cytogenetic approaches to mouse models of human genetic diseases.

@en

prefLabel

Cytogenetic approaches to mouse models of human genetic diseases.

@ast

Cytogenetic approaches to mouse models of human genetic diseases.

@en

P1476

Cytogenetic approaches to mouse models of human genetic diseases.

@en

P2093

U Francke

http://www.w3.org/2001/XMLSchema#string

P2860

Gene mapping in Mus musculus by interspecific cell hybridization: assignment of the genes for tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2

Assignment of the gene for cytoplasmic superoxide dismutase (Sod-1) to a region of chromosome 16 and of Hprt to a region of the X chromosome in the mouse

Primary defect in copper transport underlies mottled mutants in the mouse

Assignment of genes to regions of mouse chromosomes.

Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation

Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.

Homologous genes for enolase, phosphogluconate dehydrogenase, phosphoglucomutase, and adenylate kinase are syntenic on mouse chromosome 4 and human chromosome 1p.

Genetic control of morphogenetic and biochemical differentiation: lethal albino deletions in the mouse.

X-linked ichthyosis due to steroid-sulphatase deficiency.

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.

P304

S41-51

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P407

English

P433

3 Suppl

http://www.w3.org/2001/XMLSchema#string

P478

101

http://www.w3.org/2001/XMLSchema#string

P577

1980-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

7192937

http://www.w3.org/2001/XMLSchema#string

P932

1903624

http://www.w3.org/2001/XMLSchema#string