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

Prenatal diagnosis of Greig cephalopolysyndactyly syndrome: a case report.

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

Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.

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

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

A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient.

Localization of the t(2;13) breakpoint of alveolar rhabdomyosarcoma on a physical map of chromosome 2.

Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13.

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Isolation of a yeast artificial chromosome clone that spans the (12;16) translocation breakpoint characteristic of myxoid liposarcoma.

A physical map around the retinoblastoma gene.

A specific chromosome breakpoint associated with mouse plasmacytomas.

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

A physical map of human chromosome 10 and a comparison with an existing genetic map.

Mapping movements within a moving motor map.

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

Herniation of the gallbladder within a hernia of the abdominal wall associated with Mirizzi Syndrome.

Border health spans the continent.

Towards a physical map of the Drosophila melanogaster genome: mapping of cosmid clones within defined genomic divisions.

Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.

Physical map of the Listeria monocytogenes chromosome.

Physical map of the BK virus genome.

Physical map of the recA gene.

Physical map of the Myxococcus xanthus chromosome.

Suggest Documents

Prenatal diagnosis of Greig cephalopolysyndactyly syndrome: a case report.

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

Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.

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

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

A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient.

Localization of the t(2;13) breakpoint of alveolar rhabdomyosarcoma on a physical map of chromosome 2.

Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13.

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Isolation of a yeast artificial chromosome clone that spans the (12;16) translocation breakpoint characteristic of myxoid liposarcoma.

A physical map around the retinoblastoma gene.

A specific chromosome breakpoint associated with mouse plasmacytomas.

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

A physical map of human chromosome 10 and a comparison with an existing genetic map.

Mapping movements within a moving motor map.

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

Herniation of the gallbladder within a hernia of the abdominal wall associated with Mirizzi Syndrome.

Border health spans the continent.

Towards a physical map of the Drosophila melanogaster genome: mapping of cosmid clones within defined genomic divisions.

Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.

Physical map of the Listeria monocytogenes chromosome.

Physical map of the BK virus genome.

Physical map of the recA gene.

Physical map of the Myxococcus xanthus chromosome.

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

Recommend Documents

Follow Us