Identification of marker chromosomes in thirteen patients using FISH probing

Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene

1992 • 229 citations

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

1992 • 213 citations

The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype

1981 • 204 citations

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.

1991 • 169 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

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

1993 • 79 citations

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

1990 • 77 citations

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

1993 • 75 citations

Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes

1993 • 52 citations

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

1992 • 41 citations

The majority of the marker chromosomes in Japanese patients with stigmata of turner syndrome are derived from Y chromosomes

1992 • 40 citations

Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis

1993 • 16 citations

Trisomy 8p: unusual origin detected by fluorescence in situ hybridization

1992 • 7 citations