(Q28216207)

1

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Gloria T Haskell

2

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Naina Bhasin

3

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James M Lee

4

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Andrew A Gassman

5

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Jeffrey A Lieberman

6

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Anthony-Samuel LaMantia

Mechanisms of Development

7

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language of work or name

English

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publication date

February 2002

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published in

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volume

111

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issue

1-2

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page(s)

177-80

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cites work

Characterization of the opposite-strand genes from the mouse bidirectionally transcribed HTF9 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

1 reference

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7 January 2021

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

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https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

The ran GTPase regulates mitotic spindle assembly.

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https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

Mesenchymal/epithelial induction mediates olfactory pathway formation.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryos

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https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

The 22q11 deletion syndromes

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https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900616-5

7 January 2021

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

1 reference

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7 January 2021