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

Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.

A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias.

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

Could acrocallosal syndrome and Greig syndrome affect the same developmental gene?

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

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Prenatal diagnosis of Greig cephalopolysyndactyly syndrome: a case report.

Urogenital development in Pallister-Hall syndrome is disrupted in a cell-lineage-specific manner by constitutive expression of GLI3 repressor.

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.

Hemolytic uremic syndrome in families.

How gene families evolve.

A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.

Adenoid cystic carcinoma: emerging role of translocations and gene fusions.

Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome.

Two families with Alport's syndrome.

Detection of Folliculin Gene Mutations in Two Chinese Families with Birt-Hogg-Dube Syndrome.

6q21-22 deletion syndrome with interrupted aortic arch.

Interrupted aortic arch presenting as Horner's syndrome: an unusual presentation.

Neu Laxova syndrome in two Egyptian families.

TDP2 suppresses chromosomal translocations induced by DNA topoisomerase II during gene transcription.

Physiology in conservation translocations.

Characterization of Robertsonian translocations by using fluorescence in situ hybridization.

Epithelioid hemangioendotheliomas with TFE3 gene translocations are compossible with CAMTA1 gene rearrangements.

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

Suggest Documents

Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.

A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias.

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

Could acrocallosal syndrome and Greig syndrome affect the same developmental gene?

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

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Prenatal diagnosis of Greig cephalopolysyndactyly syndrome: a case report.

Urogenital development in Pallister-Hall syndrome is disrupted in a cell-lineage-specific manner by constitutive expression of GLI3 repressor.

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.

Hemolytic uremic syndrome in families.

How gene families evolve.

A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.

Adenoid cystic carcinoma: emerging role of translocations and gene fusions.

Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome.

Two families with Alport's syndrome.

Detection of Folliculin Gene Mutations in Two Chinese Families with Birt-Hogg-Dube Syndrome.

6q21-22 deletion syndrome with interrupted aortic arch.

Interrupted aortic arch presenting as Horner's syndrome: an unusual presentation.

Neu Laxova syndrome in two Egyptian families.

TDP2 suppresses chromosomal translocations induced by DNA topoisomerase II during gene transcription.

Physiology in conservation translocations.

Characterization of Robertsonian translocations by using fluorescence in situ hybridization.

Epithelioid hemangioendotheliomas with TFE3 gene translocations are compossible with CAMTA1 gene rearrangements.

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

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

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