Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue (Q28138945)

Issues in searching molecular sequence databases

GOA release 2020-03-11

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N G Pasteris

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K Nagata

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A Hall

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J L Gorski

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language of work or name

English

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publication date

25 January 2000

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published in

Gene

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volume

242

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issue

1-2

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page(s)

237-47

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Faciogenital dysplasia protein (FGD1) and Vav, two related proteins required for normal embryonic development, are upstream regulators of Rho GTPases

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Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor

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Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene.

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Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene.

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Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues

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