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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,
The GLI-Kruppel family of human genes.
1988,
Pubmed Ruppert,
GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.
1990,
Pubmed
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Xenbase Tommerup,
A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome.
1983,
Pubmed Vortkamp,
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.
1991,
Pubmed
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Xenbase Vortkamp,
A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p.
1991,
Pubmed 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
