Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.
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References (22)
A simple technique for demonstrating centromeric heterochromatin
1972 • 4,206 citations
Visualization of nucleolar organizer regions in mammalian chromosomes using silver staining
1975 • 1,131 citations
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.
1989 • 261 citations
Does ?ring syndrome? exist? An analysis of 207 case reports on patients with a ring autosome
1987 • 252 citations
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.
1990 • 241 citations
Molecular genetic approach to the characterization of the ?Down syndrome region? of chromosome 21
1989 • 195 citations
Mutation rates of structural chromosome rearrangements in man.
1981 • 137 citations
A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis
1991 • 124 citations
Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome.
1991 • 87 citations
Clinical diagnosis of Down's syndrome
1976 • 86 citations
A genetic linkage map of 27 markers on human chromosome 21
1991 • 79 citations
Cloning and expression of the human S100 beta gene.
1990 • 76 citations
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker
1990 • 60 citations
Molecular mechanism in the formation of a human ring chromosome 21.
1989 • 51 citations
[On the duplication of circular structures].
1968 • 38 citations
A case of partial monosomy 21q22.2 associated with Rieger's syndrome.
1984 • 34 citations
Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat
1990 • 29 citations
Prenatal detection of an unstable ring 21 chromosome
1984 • 23 citations
Dinucleotide repeat polymorphism located at D21S120
1990 • 23 citations
A case of r(21) with stigmata of atypical Down syndrome
1980 • 19 citations
Familial transmission of a ring chromosome 21
1987 • 16 citations
Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.
1990 • 15 citations