A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene (Q28263330)

Greig cephalopolysyndactyly syndrome

GOA release 2020-03-11

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C C Hui

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A L Joyner

series ordinal

2

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publication date

March 1993

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language of work or name

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3

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issue

3

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page(s)

241-6

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cites work

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Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.

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GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity

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GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

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The GLI gene encodes a nuclear protein which binds specific sequences in the human genome

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A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family

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Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

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The human PAX6 gene is mutated in two patients with aniridia

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The tra-1 gene determines sexual phenotype cell-autonomously in C. elegans

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