(Q28139165)

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Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation

scientific article (publication date: December 2000)

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Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation (English)

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A A Thompson

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L T Nguyen

series ordinal

2

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language of work or name

English

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publication date

December 2000

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published in

Nature Genetics

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volume

26

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issue

4

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page(s)

397-8

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cites work

Arm anomalies and bone marrow failure may go hand in hand

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reference URL

https://api.crossref.org/works/10.1038%2F82511

retrieved

21 January 2018

Homeobox genes in embryogenesis and pathogenesis

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21 January 2018

The role of HOX homeobox genes in normal and leukemic hematopoiesis

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reference URL

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retrieved

21 January 2018

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

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reference URL

https://api.crossref.org/works/10.1038%2F82511

retrieved

21 January 2018

Mutation of HOXA13 in hand-foot-genital syndrome

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21 January 2018

Genetic interactions of Hox genes in limb development: learning from compound mutants.

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21 January 2018

Homeotic transformations and limb defects in Hox A11 mutant mice.

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retrieved

21 January 2018

Overexpression of HOXA10 in murine hematopoietic cells perturbs both myeloid and lymphoid differentiation and leads to acute myeloid leukemia

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reference URL

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retrieved

21 January 2018

The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F82511

retrieved

21 January 2018

A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.

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Crossref

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21 January 2018

Thrombocytopenia and absent radius (TAR) syndrome

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21 January 2018

Developmental biology of hematopoiesis

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reference URL

https://api.crossref.org/works/10.1038%2F82511

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7 January 2021

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(Q28139165)

Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation

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