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De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH

By Serdar Kasakyan, Laurence Lohmann, Azeddine Aboura, Mazin Quimsiyeh, Yves Menezo, Gerard Tachdjian and Moncef Benkhalifa
Topics: Research
Publisher: BioMed Central
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Provided by: PubMed Central
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    1. (2006). A: Pregnancy outcomes after assisted reproductive technology.
    2. (1976). Adessa GM: Partial trisomy 9 with resemblance to Coffin-Siris syndrome.
    3. (2002). AG: High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.
    4. (2006). Application of array-base comparative genomic hybridization to clinical diagnostics.
    5. B: A cytogenetic perspective on genomic microarray.
    6. (1998). Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    7. (1997). de Martinville B: Prenatal diagnosis of partial trisomy 9p. J Gynecol Obstet Biol Reprod
    8. (1998). DG: High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet
    9. (1982). Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet
    10. (2002). G: A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9). Fetal Diagn Ther
    11. (2001). Gene expression studies on human primordial germ cells and preimplantation embryos.
    12. (2002). Giltay JC: Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
    13. (2001). Height resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 ( NF2) patient using microarrays-CGH. Hum Mol Genet
    14. (1997). Intracytoplasmic sperm injection pregnancy with fetal trisomy 9p resulting from a balanced paternal translocation. Hum Reprod
    15. (2003). JA: Array-based comparative genomic hybridization for the genome wide detection of submicroscopic chromosomal abnormalities.
    16. (1999). JC: Prenatal Diagnosis of Bilateral Ventriculomegaly and an Enlarged Cisterna Magna in a Fetus with Partial Trisomy 9 and Partial Trisomy 21. Prenat Diagn
    17. (1999). JM: An unusual presentation of trisomy 9p syndrome with a partial Dandy-Walker malformation.
    18. (2004). Kahraman S: Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture. Prenat Diagn
    19. (2004). Kalousek D: Abnormal embryonic development diagnosed embryoscopically in early intrauterine deaths after in vitro fertilization: a preliminary report of 23 cases. Fertil Steril
    20. (1997). Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer
    21. (2006). Medical application of array CGHand the transformation ofclinical cytogenetics. Cytogenet Genome Res
    22. (2006). Meijer G: BAC to the future or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH). Nucleic Acids Res
    23. (1976). Mikelsaar RV: A case of trisomy for the short arm of chromosome 9(+9p). Hum Genet
    24. (1996). Milunsky A: Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).
    25. (2002). Neonatal data on a cohort of 2889 infants born after ICSI (1991–1999) and of 2995 infants born after IVF (1983–1999). Hum Reprod
    26. (2004). NP: Microarray based comparative genomic hybridisation (arrayCGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.
    27. (2002). O: 20-Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: narrowing of the 9p duplication critical region to 6 Mb.
    28. (2004). Ouwerkek E, Meijer G, YIstra B: High resolution microarray comparative genomic hybridisation analysis using spotted oligonucleotides.
    29. (1979). Partial trisomy 9. Clinical and cytogenetic correlations. Ann Génét
    30. (2005). Prenatal diagnosis by array-CGH.
    31. (2004). Prenatal karyotypes of fetuses c conceived by intracytoplasmic sperm injection. Fetil Steril
    32. (2005). Qumsiyeh MB: Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro. Prentat Diagnosis
    33. (2003). Rare congenital disorders, imprinted genes, and assisted reproductive technology. Lancet
    34. (1995). Rodesch F: Sex chromosome abnormalities after intracytoplasmic sperm injection. Lancet
    35. (1998). S: Direct duplication of 9p22 → p24 in a child with duplication 9p syndrome.
    36. (2005). Somatic chromosomal abnormalities in infertile men and women. Cytogenet Genome Res
    37. (2005). Szuhai K: Rapid detection of genomic imbalances using micro-arrays consisting of pooled BACs covering all human chromosomes arms. Nucleics Acid Re
    38. (2006). Tachdjian G: De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterized by microarray CGH in a fetus with an increased nuchal translucency. Prenatal Diagnosis
    39. (2004). The performance of CGH array for the detection of cryptic constitutional chromosome imbalances.
    40. (2004). The results of cytogenetics analysis with regard to intracytoplasmic sperm injection in males, females and fetuses. Fetal Diagn Ther
    41. (2002). Tzen CY: Prenatal diagnosis of the DandyWalker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion. Prenat Diagn
    42. (2004). YIstra B: Microarray-based comparative genomic hybridization and it's application in human genetics. Clin Genet

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