(Q55670532)

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

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title

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

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M Gessler

2

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author name string

A Vortkamp

series ordinal

1

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K H Grzeschik

series ordinal

3

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language of work or name

English

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publication date

8 August 1991

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published in

Nature

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volume

352

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page(s)

539-40

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issue

6335

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exact match

https://scigraph.springernature.com/pub.10.1038/352539a0

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cites work

The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature

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reference URL

https://api.crossref.org/works/10.1038%2F352539A0

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7 January 2021

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

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F352539A0

retrieved

7 January 2021

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

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reference URL

https://api.crossref.org/works/10.1038%2F352539A0

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7 January 2021

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The GLI-Kruppel family of human genes

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reference URL

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7 January 2021

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

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7 January 2021

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

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https://api.crossref.org/works/10.1038%2F352539A0

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7 January 2021

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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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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F352539A0

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7 January 2021

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

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F352539A0

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7 January 2021

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Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

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7 January 2021

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Retinoids and vertebrate limb pattern formation

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stated in

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reference URL

https://api.crossref.org/works/10.1038%2F352539A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F352539A0

retrieved

7 January 2021

based on heuristic

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F352539A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

1 reference

https://api.crossref.org/works/10.1038%2F352539A0

retrieved

7 January 2021

based on heuristic

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Identifiers

DOI

10.1038/352539A0

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Dimensions Publication ID

1040461468

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PubMed ID

1650914

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ResearchGate publication ID

21504650

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(Q55670532)

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

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