(Q46056592)

19 December 2017

title

Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18. (English)

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19 December 2017

author name string

X Li

1

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19 December 2017

L Pereira

2

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19 December 2017

H Zhang

3

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19 December 2017

C Sanguineti

4

1 reference

19 December 2017

F Ramirez

5

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19 December 2017

J Bonadio

6

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19 December 2017

U Francke

7

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19 December 2017

publication date

1 December 1993

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19 December 2017

published in

Genomics

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19 December 2017

volume

18

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19 December 2017

issue

3

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19 December 2017

page(s)

667-672

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19 December 2017

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

The skipping of constitutive exons in vivo induced by nonsense mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Homogeneously staining chromosome regions and double minutes in a mouse adrenocortical tumor cell line

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Comparative chromosome mapping of a conserved homoeo box region in mouse and human

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Partial sequence of a candidate gene for the Marfan syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Gene for lymphoid enhancer-binding factor 1 (LEF1) mapped to human chromosome 4 (q23–q25) and mouse chromosome 3 near Egf

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

A system of nomenclature for band patterns of mouse chromosomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980371-4

7 January 2021

10.1016/S0888-7543(05)80371-4

Identifiers

DOI

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19 December 2017

1 reference

19 December 2017