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Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique.
Hum Genet. 1986 Aug;73(4):298-300
PMID: 2427434
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Evidence for lack of specificity of the DA/DAPI technique.
Cytogenet Cell Genet. 1987;45(1):62
PMID: 2439258
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Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15.
Chromosoma. 1985;93(1):77-86
PMID: 2998709
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A simple method of reducing the fading of immunofluorescence during microscopy.
J Immunol Methods. 1981;43(3):349-50
PMID: 7019347
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Prader-Willi syndrome and a bisatellited derivative of chromosome 15.
Clin Genet. 1980 Jul;18(1):42-7
PMID: 7418253
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Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.
J Med Genet. 1990 Mar;27(3):155-9
PMID: 2325088
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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.
Anal Biochem. 1984 Feb;137(1):266-7
PMID: 6329026
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18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence.
Hum Genet. 1986 Feb;72(2):185-7
PMID: 3753696
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Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities.
J Ment Defic Res. 1980 Dec;24 Pt 4:235-42
PMID: 7218339
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The genetic significance of accessory bisatellited marker chromosomes.
Hum Genet. 1983;65(2):155-64
PMID: 6228512
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Autistic disorder and additional inv dup(15)(pter----q13) chromosome.
Am J Med Genet. 1990 Mar;35(3):447-8
PMID: 2353962
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Lack of specificity of DA/DAPI fluorescence.
Clin Genet. 1990 Jan;37(1):74-7
PMID: 2302826
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The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.
Am J Hum Genet. 1990 Sep;47(3):493-8
PMID: 2393023
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High resolution pattern of an inverted duplication (15).
Clin Genet. 1986 Mar;29(3):241-5
PMID: 3457663
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Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.
Chromosoma. 1981;83(3):431-9
PMID: 7273954
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Preferential maternal derivation in inv dup(15): analysis of eight new cases.
Hum Genet. 1981;57(4):345-50
PMID: 7286973
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C bands in human metaphase chromosomes treated by barium hydroxide.
Ann Genet. 1974 Jun;17(2):135-6
PMID: 4139928
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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.
Proc Natl Acad Sci U S A. 1986 May;83(9):2934-8
PMID: 3458254
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Visualization of nucleolar organizer regions im mammalian chromosomes using silver staining.
Chromosoma. 1975 Nov 20;53(1):37-50
PMID: 53131
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Identification of human chromosomes by DNA-binding fluorescent agents.
Chromosoma. 1970;30(2):215-27
PMID: 4193398
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Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15.
Genomics. 1990 Jun;7(2):143-51
PMID: 1971806
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Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.
Exp Cell Res. 1978 Feb;111(2):327-32
PMID: 75107
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Forty four probands with an additional "marker" chromosome.
Hum Genet. 1985;69(4):353-70
PMID: 3857214
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Classical Prader-Willi syndrome with trisomy 15(pter----q12) plus de novo variant 15p11.
Ann Genet. 1989;32(1):39-42
PMID: 2751247
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Infertility associated with two accessory bisatellited chromosomes.
Hum Genet. 1986 Jun;73(2):133-6
PMID: 3459705
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Minute chromosomes replacing the Y chromosome carry Y-specific sequences by restriction fragment analysis and in situ hybridization.
Am J Med Genet. 1985 Oct;22(2):361-74
PMID: 2996350
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Characterization of the supernumerary chromosome in cat eye syndrome.
Science. 1986 May 2;232(4750):646-8
PMID: 3961499
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DA/DAPI heteromorphisms in acrocentric chromosomes other than 15.
Cytogenet Cell Genet. 1988;47(1-2):104-5
PMID: 2451581
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Chromosome survey of total population of mentally subnormal in North-East of Scotland.
J Med Genet. 1976 Aug;13(4):295-306
PMID: 134160
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A rapid banding technique for human chromosomes.
Lancet. 1971 Oct 30;2(7731):971-2
PMID: 4107917