Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA
Authors (first, second and last of 5)
Volume 1, issue 1, December 2008
28 articles in this issue
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De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH
Authors (first, second and last of 7)
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Chromosome distribution in human sperm – a 3D multicolor banding-study
Authors (first, second and last of 9)
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Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report
Authors (first, second and last of 11)
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Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH
Authors (first, second and last of 23)
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Rapid and reliable diagnosis of murine myeloid leukemia (ML) by FISH of peripheral blood smear using probe of PU. 1, a candidate ML tumor suppressor
Authors (first, second and last of 6)
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Unusually stable abnormal karyotype in a highly aggressive melanoma negative for telomerase activity
Authors (first, second and last of 10)
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Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report
Authors (first, second and last of 11)
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Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases
Authors (first, second and last of 4)
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Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding
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Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement
Authors (first, second and last of 9)
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Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
Authors (first, second and last of 10)
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Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature
Authors (first, second and last of 10)
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Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them
Authors (first, second and last of 7)
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Genome profiling of ovarian adenocarcinomas using pangenomic BACs microarray comparative genomic hybridization
Authors (first, second and last of 6)
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Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon
Authors (first, second and last of 7)
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Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
Authors (first, second and last of 16)
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Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization
Authors (first, second and last of 8)
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Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?
Authors (first, second and last of 13)
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An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)
Authors (first, second and last of 4)
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A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man
Authors (first, second and last of 6)
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A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics
Authors (first, second and last of 5)
