(Q28263330)

Greig cephalopolysyndactyly syndrome

GOA release 2020-03-11

1 reference

C C Hui

1

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A L Joyner

series ordinal

2

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language of work or name

English

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publication date

March 1993

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published in

Nature Genetics

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volume

3

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issue

3

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page(s)

241-6

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cites work

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

1 reference

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

21 April 2017

1 reference

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

21 April 2017

1 reference

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

21 April 2017

1 reference

Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

21 April 2017

1 reference

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 April 2017

1 reference

Mouse small eye results from mutations in a paired-like homeobox-containing gene

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

The Greig polysyndactyly-craniofacial dysmorphism syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Familial polysyndactyly and craniofacial anomalies.

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Greig cephalopolysyndactyly: report of 13 affected individuals in three families.

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

The GLI gene is a member of the Kruppel family of zinc finger proteins.

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

The GLI-Kruppel family of human genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Cloning and characterization of the segment polarity gene cubitus interruptus Dominant of Drosophila

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Molecular analysis of the C. elegans sex-determining gene tra-1: a gene encoding two zinc finger proteins

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

The GLI gene encodes a nuclear protein which binds specific sequences in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Occurrences and linkage relations of the mutant ‘extra-toes’ in the mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Brachyphalangy, an allele of extra-toes in the mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0393-241

1 reference

7 January 2021

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

The human PAX6 gene is mutated in two patients with aniridia

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

The tra-1 gene determines sexual phenotype cell-autonomously in C. elegans

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Polydactyly Nagoya, Pdn: A new mutant gene in the mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021

Expression during embryogenesis of a mouse gene with sequence homology to the Drosophila engrailed gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-241

7 January 2021