Preimplantation Genetic Diagnosis by Fluorescence In Situ Hybridization: Clinical Possibilities and Pitfalls

[1]  R. Williamson,et al.  Birth of a healthy infant after preimplantation confirmation of euploidy by comparative genomic hybridization. , 2001, The New England journal of medicine.

[2]  K. Tsuchiya,et al.  Familial X centromere variant resulting in false‐positive prenatal diagnosis of monosomy X by interphase FISH , 2001, Prenatal diagnosis.

[3]  J Cohen,et al.  Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage. , 2001, Human reproduction.

[4]  P. N. Rao,et al.  Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2‐year multi‐center retrospective study and review of the literature , 2001, Prenatal diagnosis.

[5]  P. Hunt,et al.  To err (meiotically) is human: the genesis of human aneuploidy , 2001, Nature Reviews Genetics.

[6]  A. Mercader,et al.  Clinical experience employing co-culture of human embryos with autologous human endometrial epithelial cells. , 2000, Human reproduction.

[7]  L. Gianaroli,et al.  Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed. , 1999, Fertility and sterility.

[8]  M. Rocchi,et al.  Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21. , 1999, Genome research.

[9]  L. Gianaroli,et al.  Positive outcome after preimplantation diagnosis of aneuploidy in human embryos. , 1999, Human reproduction.

[10]  C. Rubio,et al.  In vitro fertilization plus preimplantation genetic diagnosis in patients with recurrent miscarriage: an analysis of chromosome abnormalities in human preimplantation embryos. , 1999, Fertility and sterility.

[11]  Jacques Cohen,et al.  Preimplantation Genetic Diagnosis of Aneuploidy: Were We Looking at the Wrong Chromosomes? , 1999, Journal of Assisted Reproduction and Genetics.

[12]  A. Handyside,et al.  Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis , 1998, Prenatal diagnosis.

[13]  P. Devroey,et al.  Successful preimplantation genetic diagnosis is related to the number of available cumulus-oocyte complexes. , 1998, Human reproduction.

[14]  U. Eichenlaub-Ritter.  Genetics of oocyte ageing. , 1998, Maturitas.

[15]  C. Strom,et al.  Preimplantation Diagnosis of Common Aneuploidies by the First- and Second-Polar Body FISH Analysis , 1998, Journal of Assisted Reproduction and Genetics.

[16]  L. Gianaroli,et al.  Incidence of Chromosomal Abnormalities from a Morphologically Normal Cohort of Embryos in Poor-Prognosis Patients , 1998, Journal of Assisted Reproduction and Genetics.

[17]  C. Simón,et al.  FISH Preimplantation Diagnosis of Chromosome Aneuploidy in Recurrent Pregnancy Wastage , 1998, Journal of Assisted Reproduction and Genetics.

[18]  J. Cohen,et al.  First pregnancies after preconception diagnosis of translocations of maternal origin. , 1998, Fertility and sterility.

[19]  L. Gianaroli,et al.  Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy? , 1997, Human reproduction.

[20]  Y. Ménézo,et al.  Maternal age effect on early human embryonic development and blastocyst formation , 1996, Molecular reproduction and development.

[21]  J. Grifo,et al.  Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities. , 1995, Fertility and sterility.

[22]  R J Sherins,et al.  Intracytoplasmic sperm injection facilitates fertilization even in the most severe forms of male infertility: pregnancy outcome correlates with maternal age and number of eggs available. , 1995, Fertility and sterility.

[23]  R. Slotnick,et al.  Preimplantation genetic diagnosis for Tay-Sachs disease: successful pregnancy after pre-embryo biopsy and gene amplification by polymerase chain reaction. , 1995, Fertility and sterility.

[24]  L. Regan,et al.  An informative protocol for the investigation of recurrent miscarriage: preliminary experience of 500 consecutive cases. , 1994, Human reproduction.

[25]  J. Connor,et al.  The chromosome constitution of human preimplantation embryos fertilized in vitro. , 1994, Human reproduction.

[26]  C. Tyler-Smith,et al.  Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes , 1993, Nature Genetics.

[27]  Z. Rosenwaks,et al.  Diagnosis of major chromosome aneuploidies in human preimplantation embryos. , 1993, Human reproduction.

[28]  D. Griffin,et al.  Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH). , 1993, Human molecular genetics.

[29]  A. Handyside,et al.  Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis. , 1992, The New England journal of medicine.

[30]  I. Sargent,et al.  Trophectoderm biopsy in human blastocysts. , 1990, Human reproduction.

[31]  G. Stirrat.  Recurrent miscarriage II: clinical associations, causes, and management , 1990, The Lancet.

[32]  A. Handyside,et al.  Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage. , 1990, Human reproduction.

[33]  M. Braekeleer,et al.  Cytogenetic studies in couples experiencing repeated pregnancy losses. , 1990, Human reproduction.

[34]  A. H. Handyside,et al.  Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification , 1990, Nature.

[35]  J. Mandelbaum,et al.  Chromosome investigations in early life. I. Human oocytes recovered in an IVF programme. , 1986, Human reproduction.

[36]  C. Coulam.  Unexplained Recurrent Pregnancy Loss: Epilogue , 1986, Clinical obstetrics and gynecology.

[37]  D. Warburton,et al.  The relationship between maternal age and chromosome size in autosomal trisomy. , 1986, American journal of human genetics.

[38]  P. Jacobs,et al.  A cytogenetic study of spontaneous abortions in Hawaii , 1978, Annals of human genetics.

[39]  J. Boué,et al.  Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions. , 1976, Teratology.

[40]  J. Boué,et al.  Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions , 1975 .

[41]  S. Munné.  Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. , 2002, Reproductive biomedicine online.

[42]  Z. Rosenwaks,et al.  CLINICAL ASSISTED REPRODUCTION An Analysis of the Effect of Age on Implantation Rates , 2000 .

[43]  J. Harper,et al.  Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions , 1998, Human Genetics.

[44]  C. Rubio,et al.  Increased chromosome abnormalities in human preimplantation embryos after in-vitro fertilization in patients with recurrent miscarriage. , 1998, Reproduction, fertility, and development.

[45]  J. Delhanty,et al.  The origin of genetic defects in the human and their detection in the preimplantation embryo. , 1995, Human reproduction update.

[46]  J. Wauters,et al.  Incidence of low-fluorescence alpha satellite region on chromosome 21 escaping detection of aneuploidy at interphase by FISH. , 1995, Cytogenetics and cell genetics.

[47]  D. Griffin,et al.  Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes. , 1991, Human reproduction.