Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis
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E. Sala | L. Dalprà | P. Riva | N. Villa | F. Crosti | S. Mariani | D. Colombo | C. Zorloni
[1] R. Tenconi,et al. NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes. , 2000, American journal of human genetics.
[2] N. Rubtsov,et al. Characterization of a small supernumerary ring marker derived from chromosome 2 by forward and reverse chromosome painting. , 1999, American journal of medical genetics.
[3] J. Crolla. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature. , 1998, American journal of medical genetics.
[4] M. Mattéi,et al. Clinical Heterogeneity in 16 Patients with inv dup 15 Chromosome: Cytogenetic and Molecular Studies, Search for an Imprinting Effect , 1996, European journal of human genetics : EJHG.
[5] J. Nelson,et al. Identification of marker chromosomes in thirteen patients using FISH probing. , 1994, American journal of medical genetics.
[6] L. Dalprà,et al. ‘Late’ chorionic villus sampling: Cytogenetic aspects , 1993, Prenatal diagnosis.
[7] D. Porteous,et al. YAC mapping by FISH using Alu-PCR-generated probes. , 1992, Genomics.
[8] D. Warburton,et al. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. , 1991, American journal of human genetics.
[9] J. Yates,et al. Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses , 1984, Prenatal diagnosis.