(Q57927095)

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Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)

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scholarly article

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Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) (English)

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Greig cephalopolysyndactyly syndrome

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Manfred Gessler

object named as

Manfred Gessler

3

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author name string

A Vortkamp

1

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T Franz

2

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M Gessler

3

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K H Grzeschik

4

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Andrea Vortkamp

1

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Thomas Franz

2

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Karl Heinz Grzeschik

4

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language of work or name

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publication date

1992

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number of pages

3

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Mammalian Genome

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3

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461-3

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461-463

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8

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https://scigraph.springernature.com/pub.10.1007/bf00356157

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Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

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https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

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inferred from PubMed ID database lookup

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

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https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription of H-2 and Qa genes in embryonic and adult mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The GLI-Kruppel family of human genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1322743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00356157

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