Comparative Genomic Hybridization for Cytogenetic Evaluation of Stillbirth
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[1] G. Feldman. Prospective risk of stillbirth , 1992, BMJ : British Medical Journal.
[2] José María Sánchez,et al. Cytogenetic study of spontaneous abortions by transabdominal villus sampling and direct analysis of villi , 1999, Prenatal diagnosis.
[3] G. Barkai,et al. Detection of numerical chromosome aberrations by comparative genomic hybridization , 1999, Prenatal diagnosis.
[4] K. Hirschhorn,et al. Clinical applications of comparative genomic hybridization , 1998, Genetics in Medicine.
[5] L. Shulman,et al. Primed in situ labeling for rapid prenatal diagnosis. , 1998, American journal of obstetrics and gynecology.
[6] O. Kallioniemi,et al. Genome screening by comparative genomic hybridization. , 1997, Trends in genetics : TIG.
[7] G. Stetten,et al. New cytogenetic technology and its application in maternal-fetal medicine , 1997 .
[8] D. Ledbetter,et al. A complete set of human telomeric probes and their clinical application , 1996, Nature Genetics.
[9] E. Schröck,et al. PARTIAL TRISOMY/MONOSOMY 6q IN FETAL CELLS AND CVS LONG‐TERM CULTURE NOT PRESENT IN CVS SHORT‐TERM CULTURE , 1996, Prenatal diagnosis.
[10] C. Lundsteen,et al. Comparative genomic hybridization in clinical cytogenetics. , 1995, American journal of human genetics.
[11] R. Falk,et al. Prenatal identification of i(YP) by molecular cytogenetic analysis , 1994, Prenatal diagnosis.
[12] J Piper,et al. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors , 1994, Genes, chromosomes & cancer.
[13] R. Pauli,et al. Wisconsin Stillbirth Service Program: II. Analysis of diagnoses and diagnostic categories in the first 1,000 referrals. , 1994, American journal of medical genetics.
[14] D. Pinkel,et al. Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors , 2022 .
[15] Feldman Gb. Prospective risk of stillbirth. , 1992 .
[16] R. Pitkin. Fetal death: diagnosis and management. , 1987, American journal of obstetrics and gynecology.
[17] H. Willard,et al. Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation. , 1986, Nucleic acids research.
[18] T. Macpherson,et al. Predicting in vitro tissue culture growth for cytogenetic evaluation of stillborn fetuses. , 1985, European journal of obstetrics, gynecology, and reproductive biology.
[19] A. Sandison,et al. Chromosome variation in perinatal mortality: a survey of 500 cases. , 1984, Journal of medical genetics.
[20] Z. Brown,et al. Evaluation of a protocol for post-mortem examination of stillbirths. , 1983, The New England journal of medicine.
[21] G. Sutherland,et al. Cytogenetic studies: an essential part of the paediatric necropsy. , 1983, Journal of clinical pathology.
[22] J. Hindley,et al. Cloning of human satellite III DNA: different components are on different chromosomes. , 1979, Nucleic acids research.