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

Data up to Jan 2025

Published1991
Citations169
References17

Total Citations Per Year

Abstract

References (17)

High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones

1990 • 1,357 citations

Detection of bcr - abl Fusion in Chronic Myelogeneous Leukemia by in Situ Hybridization

1990 • 371 citations

Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome.

1990 • 247 citations

Clinical and molecular diagnosis of Miller-Dieker syndrome.

1991 • 232 citations

Syndromes with lissencephaly. I: Millerdieker and Norman‐Roberts syndromes and isolated lissencephaly

1984 • 222 citations

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

1990 • 213 citations

Detection of the Philadelphia chromosome in interphase nuclei

1990 • 185 citations

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

1990 • 153 citations

A highly polymorphic locus in human DNA revealed by cosmid-derived probes.

1985 • 134 citations

An improved method for G-banding chromosomes after in situ hybridization

1984 • 132 citations

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

1988 • 92 citations

Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus

1990 • 76 citations

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

1990 • 71 citations

Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction

1990 • 59 citations

Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.

1989 • 59 citations

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

1988 • 59 citations

A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes

1990 • 19 citations

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Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ… (1991) – PubMed | Metascience Observatory Explorer