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Fahrner,
Transcription of H-2 and Qa genes in embryonic and adult mice.
1987, Pubmed
Fahrner,
Transcription of H-2 and Qa genes in embryonic and adult mice.
1987,
Pubmed
Gollop,
The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
1985,
Pubmed
Johnson,
Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.
1967,
Pubmed
Krüger,
Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).
1989,
Pubmed
Kunkel,
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
1982,
Pubmed
Pettigrew,
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.
1991,
Pubmed
Pohl,
Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt).
1990,
Pubmed
Ruppert,
GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.
1990,
Pubmed
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Xenbase
Ruppert,
The GLI-Kruppel family of human genes.
1988,
Pubmed
Tommerup,
A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome.
1983,
Pubmed
Vortkamp,
A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p.
1991,
Pubmed
Vortkamp,
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.
1991,
Pubmed
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Xenbase
Wagner,
Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.
1990,
Pubmed
Winter,
Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes).
1988,
Pubmed
