De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.
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[1] J. Crane,et al. Correlation between phenotypic expression of de novo marker chromosomes and genomic organization using replicational banding , 1990, Prenatal diagnosis.
[2] E. Haan,et al. The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization. , 1990, American journal of human genetics.
[3] M. Andrews. From Eastern Virginia Medical School , 1989 .
[4] J. Tolmie,et al. Outcome of de novo balanced translocations ascertained prenatally. , 1989, Journal of medical genetics.
[5] D. Donnai. The clinical significance of de novo structural rearrangements and markers detected prenatally by amniocentesis , 1989 .
[6] E. Wassman,et al. "Possibly" de novo translocations: prenatal risk counseling. , 1989, American journal of obstetrics and gynecology.
[7] B. Emanuel,et al. Comparative mapping of the constitutional and tumor-associated 11;22 translocations. , 1989, American journal of human genetics.
[8] H. Berghe,et al. De novo Robertsonian D/D type translocations: the Leuven experience , 1989, Clinical genetics.
[9] E. Hook,et al. How much difference does chromosome banding make?: Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities , 1989, Annals of human genetics.
[10] C. Denniston,et al. The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations , 1989, Annals of human genetics.
[11] G. Sutherland,et al. No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells. , 1988, Cancer genetics and cytogenetics.
[12] J. D. den Hollander,et al. Marker chromosomes in A series of 10000 prenatal diagnoses. Cytogenetic and follow‐up studies , 1987, Prenatal diagnosis.
[13] E. Hook,et al. Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age. , 1987, American journal of human genetics.
[14] P. Cross,et al. Rates of mutant and inherited structural cytogenetic abnormalities detected at amniocentesis: results on about 63000 fetuses , 1987, Annals of human genetics.
[15] J. C. Parke,et al. Antenatal diagnosis of a de novo paracentric inversion of chromosome 11 , 1987, Prenatal diagnosis.
[16] A. Boué,et al. Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the european collaborative prenatal diagnosis centres , 1986, Prenatal diagnosis.
[17] E. Kuwertz,et al. Inv dup (15): Prenatal diagnosis and postnatal follow‐up , 1986, Prenatal diagnosis.
[18] M. Bogart,et al. Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement. , 1986, Journal of medical genetics.
[19] T. Mohandas,et al. Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis. , 1985, American journal of medical genetics.
[20] A. Boué,et al. A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses , 1984, Prenatal diagnosis.
[21] D. Warburton. Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis , 1984, Prenatal diagnosis.
[22] F. Hecht,et al. Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns , 1984, Clinical genetics.
[23] F. Hecht,et al. Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis , 1984, Clinical genetics.
[24] P. Benn,et al. Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis. , 1984, American journal of human genetics.
[25] S. Ratcliffe,et al. Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population. , 1984, Journal of medical genetics.
[26] L. Weiss,et al. The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age. , 1983, American journal of human genetics.
[27] M. Spence,et al. Mental retardation associated with "balanced" chromosome rearrangements. , 1977, American journal of human genetics.
[28] P. Jacobs. Correlation between euploid structural chromosome rearrangements and mental subnormality in humans , 1974, Nature.
[29] P. Jacobs,et al. An Analysis of the Break Points of Structural Rearrangements in Man , 1974, Journal of medical genetics.
[30] D. Miller,et al. Identification of translocation chromosomes by quinacrine fluorescence. , 1972, American journal of diseases of children.
[31] H. Barnard,et al. The Children's Hospital, Los Angeles , 1915 .
[32] James D. McKean,et al. REPORT OF THE COMMITTEE , 2005 .
[33] H. Cuckle. Antenatal diagnosis. , 1992, The Practitioner.
[34] J. Trent,et al. Report of the committee on structural chromosome changes in neoplasia. , 1989, Cytogenetics and cell genetics.
[35] D. Ledbetter,et al. Report of the committee on cytogenetic markers. , 1989, Cytogenetics and cell genetics.
[36] N. Philip,et al. [Balanced chromosome rearrangements with abnormal phenotype]. , 1988, Journal de genetique humaine.
[37] J. Trent,et al. Report of the committee on structural chromosome changes in neoplasia. , 1988, Cytogenetics and cell genetics.
[38] P. Koduru,et al. Congenital chromosome breakage clusters within Giemsa-light bands and identifies sites of chromatin instability. , 1988, Cytogenetics and cell genetics.
[39] A. Bolte,et al. [Incidence and significance of chromosomal translocations in prenatal diagnosis]. , 1986, Geburtshilfe und Frauenheilkunde.
[40] D. Warburton. DE NOVO STRUCTURAL REARRANGEMENTS: IMPLICATIONS FOR PRENATAL DIAGNOSIS , 1982 .
[41] E. J. Smith. A children's hospital in a medical center , 1947 .