(Q28593833)

31 January 2017

title

Synpolydactyly in mice with a targeted deficiency in the HoxD complex (English)

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31 January 2017

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GOA release 2020-03-11

Homeobox D13

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GOA release 2020-03-11

Homeobox D12

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GOA release 2020-03-11

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D. Duboule

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31 January 2017

J. Zákány

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31 January 2017

language of work or name

English

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publication date

7 November 1996

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31 January 2017

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31 January 2017

volume

384

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31 January 2017

issue

6604

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31 January 2017

page(s)

69–71

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Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

31 January 2017

cites work

1 reference

7 January 2021

Hox gene expression in teleost fins and the origin of vertebrate digits

1 reference

7 January 2021

Independent control of immunoglobulin switch recombination at individual switch regions evidenced through Cre-loxP-mediated gene targeting

1 reference

7 January 2021

Chromosome engineering in mice

1 reference

7 January 2021

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

1 reference

7 January 2021

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

1 reference

7 January 2021

Hox genes in vertebrate development

1 reference

7 January 2021

Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls.

1 reference

7 January 2021

Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice

1 reference

7 January 2021

Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker

1 reference

7 January 2021

Colinearity and functional hierarchy among genes of the homeotic complexes

1 reference

7 January 2021

Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: evidence for tissue-specific modulation of receptor function

1 reference

7 January 2021