Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH.

Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in �rhus, Denmark

1991 • 1,093 citations

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

1991 • 679 citations

A cytogenetic survey of 14,069 newborn infants

1975 • 560 citations

A cytogenetic survey of 11,680 newborn infants

1974 • 431 citations

Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses

1984 • 394 citations

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

1991 • 138 citations

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

1992 • 138 citations

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.

1993 • 127 citations

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

1995 • 118 citations

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization

1994 • 108 citations

Marker chromosomes in A series of 10000 prenatal diagnoses. Cytogenetic and follow‐up studies

1987 • 105 citations

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

1993 • 79 citations

Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis

1984 • 79 citations

A 10‐year survey, 1980–1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by fish analysis. Outcome and follow‐up of 14 cases diagnosed in a series of 12 699 prenatal samples

1995 • 77 citations

Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age.

1987 • 75 citations

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

1993 • 75 citations

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

1990 • 74 citations

Identification of marker chromosomes in thirteen patients using FISH probing

1994 • 46 citations

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

1995 • 40 citations

Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes

1993 • 37 citations

Development of 124 Sequence-Tagged Sites and Cytogenetic Localization of 217 Cosmids for Human Chromosome 10

1994 • 23 citations

Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies

1994 • 23 citations

Extra marker chromosome in newborn children

2009 • 23 citations

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

1993 • 21 citations

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization

1995 • 20 citations

An accessory marker derived from chromosome 20 and its co‐existence with a mosaic trisomy 20 cell line

1995 • 16 citations

Supernumerary chromosome marker (1) in a developmentally delayed child

1995 • 15 citations

A small supernumerary marker chromosome X identified by in situ hybridization

1995 • 9 citations