Characterization of a de novo 48,XX, + r(X), + r(17) by in situ hybridizatio in a patient with neurofibromatosis (NF1)

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

1991 • 138 citations

Ullrich‐Turner syndrome with a small ring X chromosome and presence of mental retardation

1992 • 95 citations

Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis

1984 • 79 citations

Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17

1989 • 66 citations

Mental retardation in Turner syndrome

1991 • 48 citations

Formation of a minichromosome by excision of the proximal region of 17q in a patient with von Recklinghausen neurofibromatosis

1990 • 30 citations

A fluorescence in situ hybridization technique for retrospective cytogenetic analysis

1991 • 28 citations

DE NOVO STRUCTURAL REARRANGEMENTS: IMPLICATIONS FOR PRENATAL DIAGNOSIS

1982 • 26 citations

Neurofibromatosis in a man with a ring 22: In situ hybridization studies

1987 • 22 citations