Wikidata

(Q28585278)

English

The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes

scientific journal article

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title
The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes (English)
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
author name string
S. Bruneau
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
K. R. Johnson
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
M. Yamamoto
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
A. Kuroiwa
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
publication date
15 September 2001
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
volume
237
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
page(s)
345–353
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017
issue
2
1 reference
stated in
PubMed
PubMed ID
11543619
retrieved
31 January 2017

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