Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES

1971 • 5,049 citations

Identification of human chromosomes by DNA-binding fluorescent agents

1970 • 989 citations

High Resolution of Human Chromosomes

1976 • 786 citations

Differential activity of maternally and paternally derived chromosome regions in mice

1985 • 708 citations

Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome

1981 • 615 citations

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1989 • 575 citations

‘Puppet’ Children A Report on Three Cases

1965 • 521 citations

Simultaneous fluorescent staining of R bands and specific heterochromatic regions (DA-DAPI bands) in human chromosomes

1980 • 468 citations

DIFFERENTIAL IMPRINTING AND EXPRESSION OF MATERNAL AND PATERNAL GENOMES

1988 • 451 citations

Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndrome

1986 • 319 citations

The β2-microglobulin gene is on chromosome 15 and not in the HL-A region

1975 • 274 citations

Quantitative analysis of high-resolution trypsin-Giemsa bands on human prometaphase chromosomes

1978 • 248 citations

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.

1982 • 238 citations

Is angelman syndrome an alternate result of del(15)(qllql3)?

1987 • 238 citations

Prader-Willi syndrome

1984 • 200 citations

Parental origin effects in mice

1986 • 175 citations

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance

1987 • 171 citations

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndrome

1989 • 164 citations

The association of Angelman's syndrome with deletions within 15q11-13.

1989 • 125 citations

Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes

1988 • 97 citations

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.

1988 • 92 citations

Prader-Willi syndrome and chromosome 15

1983 • 88 citations

Incidence of 15q deletions in the Angelman syndrome: A survey of twelve affected persons

1989 • 88 citations

Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients

1988 • 78 citations

Preferential maternal derivation in inv dup(15)

1981 • 71 citations

Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

1988 • 59 citations

Recurrence risk in the Angelman (“happy puppet”) syndrome

1987 • 48 citations

Cytogenetic and molecular study of the Angelman syndrome

1990 • 41 citations

Angelman syndrome in a daughter with del(15) (q11q13) associated with brachycephaly, hearing loss, enlarged foramen magnum, and ataxia in the mother

1989 • 32 citations

Parental origin of the extra chromosome in the cat eye syndrome: Evidence from heteromorphism and in situ hybridization analysis

1988 • 30 citations

Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry

1989 • 27 citations

Assignment of the gene for beta 2-microglobulin (B2m) to mouse chromosome 2.

1982 • 25 citations

Chapter 75 Human fetal cortices and spinal cord transplanted to the anterior chamber of immunodeficient nude rats: immunohistochemical studies

1988 • 21 citations

Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter?q21

1980 • 17 citations