Large inv dup(15) chromosome in two generations.
作者信息
Van Der Smagt J J, Giltay J C, De Ne J J, Slabbers G H
出版信息
J Med Genet. 1996 Mar;33(3):261-2. doi: 10.1136/jmg.33.3.261-a.
Abstract
摘要
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本文引用的文献
1
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
Am J Hum Genet. 1994 May;54(5):748-56.
2
Clinical and molecular analysis of five inv dup(15) patients.
Eur J Hum Genet. 1993;1(1):37-50. doi: 10.1159/000472386.
3
Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
Am J Hum Genet. 1994 Oct;55(4):753-9.
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Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.
Prenat Diagn. 1994 Nov;14(11):1019-28. doi: 10.1002/pd.1970141103.
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Inv dup(15) supernumerary marker chromosomes.
J Med Genet. 1994 Aug;31(8):585-94. doi: 10.1136/jmg.31.8.585.
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Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Am J Med Genet. 1995 Jan 2;55(1):85-94. doi: 10.1002/ajmg.1320550122.
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Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis.
Hum Genet. 1995 Feb;95(2):161-70. doi: 10.1007/BF00209395.
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Forty four probands with an additional "marker" chromosome.
Hum Genet. 1985;69(4):353-70. doi: 10.1007/BF00291656.
9
Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15.
Chromosoma. 1985;93(1):77-86. doi: 10.1007/BF01259449.
10
Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.
Hum Genet. 1991 Jul;87(3):290-6. doi: 10.1007/BF00200906.
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