Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies.
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I. Cetin | M. Miozzo | G. Simoni | F. Grati | B. Cassani | S. Sirchia | G. Bulfamante | S. Rigano | B. Gentilin | F. Rossella | P. Antonazzo | L. Mori
[1] A. Telenius,et al. Distribution of mosaicism in human placentae , 1996, Human Genetics.
[2] D. Kalousek,et al. The utilization of interphase cytogenetic analysis for the detection of mosaicism , 1994, Human Genetics.
[3] W. Robinson,et al. Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism , 2003, Journal of medical genetics.
[4] Wendy Dean,et al. Regulation of supply and demand for maternal nutrients in mammals by imprinted genes , 2003, The Journal of physiology.
[5] S. Langlois,et al. Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism , 2002, Prenatal diagnosis.
[6] D. Kidron,et al. CGH in the detection of confined placental mosaicism (CPM) in placentas of abnormal pregnancies , 2002, Prenatal diagnosis.
[7] G. Pardi,et al. Placental-fetal interrelationship in IUGR fetuses--a review. , 2002, Placenta.
[8] R. Resnik. Intrauterine growth restriction. , 2002, Obstetrics and gynecology.
[9] G. Pardi,et al. Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression. , 2001, Placenta.
[10] S. Abbs,et al. Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis , 2001, The Lancet.
[11] V. Lestou,et al. Comparative genomic hybridization: a new tool for reproductive pathology. , 2001, Archives of pathology & laboratory medicine.
[12] G. Pardi,et al. Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parameters. , 2000, Cancer genetics and cytogenetics.
[13] V. Lestou,et al. Comparative genomic hybridization: a new approach to screening for intrauterine complete or mosaic aneuploidy. , 2000, American journal of medical genetics.
[14] R. Brusati,et al. Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas. , 2000, Cancer genetics and cytogenetics.
[15] D. Kalousek. Pathogenesis of chromosomal mosaicism and its effect on early human development. , 2000, American journal of medical genetics.
[16] J. Kingdom,et al. Definitions of Intrauterine Growth Restriction , 2000 .
[17] P. Baker,et al. In trauterine growth restriction aetiology and management , 2000 .
[18] V. Lestou,et al. Screening of human placentas for chromosomal mosaicism using comparative genomic hybridization. , 1999, Teratology.
[19] V. Lestou,et al. Confined placental mosaicism and intrauterine fetal growth , 1998, Archives of disease in childhood. Fetal and neonatal edition.
[20] V. Lestou,et al. Confined placental mosaicism for chromosome 7 detected by comparative genomic hybridization , 1998, Prenatal diagnosis.
[21] A. Paoloni-Giacobino,et al. Prenatal supernumeray r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome , 1998, Prenatal diagnosis.
[22] J. Kingdom,et al. Oxygen and placental villous development: origins of fetal hypoxia. , 1997, Placenta.
[23] A. Telenius,et al. Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. , 1997, American journal of human genetics.
[24] M. Miller,et al. The use of amplified variable number of tandem repeats (VNTR) in the detection of chimerism following bone marrow transplantation. A comparison with restriction fragment length polymorphism (RFLP) by Southern blotting. , 1997, American journal of clinical pathology.
[25] P. Walsh,et al. Sequence analysis and characterization of stutter products at the tetranucleotide repeat locus vWA. , 1996, Nucleic acids research.
[26] D. Ledbetter,et al. Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. , 1995, Human molecular genetics.
[27] D. Kalousek,et al. Genomic imprinting related to prenatal diagnosis , 1994, Prenatal diagnosis.
[28] J. Wiley,et al. Confined placental mosaicism, IUGR, and adverse pregnancy outcome: A controlled retrospective U.K. collaborative survey , 1994, Prenatal diagnosis.
[29] E. Ferrazzi,et al. Diagnostic value of blood sampling in fetuses with growth retardation. , 1993, The New England journal of medicine.
[30] S. Langlois,et al. Uniparental disomy for chromosome 16 in humans. , 1993, American journal of human genetics.
[31] J. Schulman,et al. Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism , 1991, Prenatal diagnosis.
[32] E. Engel,et al. Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection. , 1991, American journal of medical genetics.
[33] L. Fedele,et al. [Standards of birth weight in Italy]. , 1991, Annali di ostetricia, ginecologia, medicina perinatale.
[34] E. Ferrazzi,et al. Doppler velocimetry: critical analysis of umbilical, cerebral and aortic reference values. , 1991, European journal of obstetrics, gynecology, and reproductive biology.
[35] S. Godfrey,et al. Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans? , 1989, American journal of human genetics.
[36] C. Redman,et al. REVISED DEFINITION OF PRE-ECLAMPSIA , 1988, The Lancet.
[37] D. Ledbetter,et al. Uniparental disomy as a mechanism for human genetic disease. , 1988, American journal of human genetics.
[38] E. Ferrazzi,et al. Fitting growth curves to head and abdomen measurements of the fetus: A multicentric study , 1987, Journal of clinical ultrasound : JCU.