Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma

Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours

1992 • 1,787 citations

Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.

1991 • 897 citations

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

1992 • 692 citations

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

1991 • 664 citations

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

1992 • 470 citations

A specific chromosomal abnormality in rhabdomyosarcoma

1987 • 326 citations

Translocations, master genes, and differences between the origins of acute and chronic leukemias

1991 • 286 citations

Consistent chromosomal translocation in alveolar rhabdomyosarcoma

1986 • 233 citations

Conservation of the paired domain in metazoans and its structure in three isolated human genes.

1989 • 210 citations

Oncogenic conversion of transcription factors by chromosomal translocations

1991 • 209 citations

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

1992 • 184 citations

Chromosomal analysis of sixteen human rhabdomyosarcomas.

1988 • 178 citations

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

1992 • 93 citations

Mapping of Col3a1 and Col6a3 to proximal murine chromosome 1 identifies conserved linkage of structural protein genes between murine chromosome 1 and human chromosome 2q

1990 • 68 citations

The host resistance locus Bcg is tightly linked to a group of cytoskeleton-associated protein genes that include villin and desmin

1991 • 36 citations

Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I

1992 • 35 citations

Molecular and cytogenetic analysis of chromosomal arms 2q and 13q in alveolar rhabdomyosarcoma

1991 • 35 citations

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

1992 • 25 citations

Chromosomal sublocalization of the 2;13 translocation breakpoint in alveolar rhabdomyosarcoma

1992 • 16 citations

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

1991 • 16 citations

Molecular definition in a somatic cell hybrid of a specific 2:13 translocation breakpoint in childhood rhabdomyosarcoma.

1991 • 11 citations