Aggressive Fibromatosis (Desmoid Tumor) is A Monoclonal Disorder

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

1992 • 1,686 citations

Hereditary cancer, oncogenes, and antioncogenes.

1985 • 1,261 citations

Langerhans'-Cell Histiocytosis (Histiocytosis X) -- A Clonal Proliferative Disease

1994 • 999 citations

Clonal analysis using recombinant DNA probes from the X-chromosome.

1987 • 439 citations

PCR bias in amplification of androgen receptor alleles, a trinucleotide repeat marker used in clonality studies

1995 • 193 citations

Coexistence of somatic and germ-line mutations of APC gene in desmoid tumors from patients with familial adenomatous polyposis.

1993 • 152 citations

Clonal chromosomal abnormalities in desmoid tumors. Implications for histopathogenesis

1992 • 151 citations

A polymerase chain reaction assay for non-random X chromosome inactivation identifies monoclonal endometrial cancers and precancers.

1995 • 106 citations

Activating mutations of Gs protein in monostotic fibrous lesions of bone

1996 • 89 citations

Novel mutations and inactivation of both alleles of the APC gene in desmoid tumors

1995 • 62 citations

Platelet‐derived growth factor in fibrous musculoskeletal disorders: A study of pathologic tissue sections and in vitro primary cell cultures

1995 • 57 citations

Some desmoid tumors are characterized by trisomy 8

1994 • 50 citations

Aggressive Fibromatosis

1992 • 43 citations

Molecular Genetic and Immunohistochemical Analysis of the Tumor Suppressor Genes Rb and p53 in Palmar and Aggressive Fibromatosis

1996 • 40 citations