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

Author

Manfred Gessler

Published in: Nature

Date of publication: August 8, 1991

Language: English

Bibliographic databases:

Cites articles 13

Date

Title

Authors

November 1983

A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome

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Genomic sequencing
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The GLI-Kruppel family of human genes

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Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.
December 1, 1988

Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes)
March 1, 1989

Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).
May 1, 1989

Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13).
August 1, 1989

Retinoids and vertebrate limb pattern formation
October 1990

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

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November 1, 1990

Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes
February 22, 1990

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
January 1, 1990

Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel

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