S P Romana

Summary

Country: France

Publications

  1. ncbi request reprint NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
    S P Romana
    Service de Cytogénétique, Centre Hospitalier Universitaire CHU Necker Enfants Malades, Paris, France
    Leukemia 20:696-706. 2006
  2. ncbi request reprint PMX2B, a new candidate gene for Hirschsprung's disease
    H K Benailly
    Département de génétique, Hopital Necker Enfants Malades, Paris, France
    Clin Genet 64:204-9. 2003
  3. ncbi request reprint Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis
    H Elghezal
    Service de Cytogénétique, Hopital Necker Enfants Malades, Paris, France
    Genes Chromosomes Cancer 30:383-92. 2001
  4. ncbi request reprint Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
    S Brisset
    Service de Cytogénétique et d Embryologie, Hopital Necker Enfants Malades, Paris, France
    Am J Med Genet 113:339-45. 2002
  5. ncbi request reprint [Microarray CGH: principle and use for constitutional disorders]
    D Sanlaville
    Service de Cytogénétique, Hopital Necker Enfants Malades, Assistance Publique Hopitaux de Paris, 149, rue de Sevres, 75015 Paris, France
    Arch Pediatr 12:1515-20. 2005
  6. ncbi request reprint The TEL gene products: nuclear phosphoproteins with DNA binding properties
    H Poirel
    U 301 de l Institut National de la Santé et de la Recherche Médicale INSERM and SD 401 No 301 CNRS, Paris, France
    Oncogene 14:349-57. 1997
  7. ncbi request reprint A CGH study of 27 patients with CHARGE association
    D Sanlaville
    Département de Génétique Hôpital Necker Enfants Malades, Paris, France
    Clin Genet 61:135-8. 2002
  8. ncbi request reprint The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
    S P Romana
    U 301 de l Institut National de la Santé et de la Recherche Médicale INSERM, Paris, France
    Blood 85:3662-70. 1995
  9. ncbi request reprint NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance
    P Ballerini
    Leukemia 19:468-70. 2005
  10. ncbi request reprint [Spectral karyotyping (SKY) principle, avantages and limitations]
    M A Belaud-Rotureau
    Service d Histologie, Embryologie et Cytogenetique, Hopital Necker Enfants Malades, Paris
    Ann Biol Clin (Paris) 61:139-46. 2003

Collaborators

Detail Information

Publications13

  1. ncbi request reprint NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
    S P Romana
    Service de Cytogénétique, Centre Hospitalier Universitaire CHU Necker Enfants Malades, Paris, France
    Leukemia 20:696-706. 2006
    ..The present study as well as a review of the 73 cases previously reported in the literature allowed us to delineate some chromosomal, clinical and molecular features of patients carrying a NUP98 gene rearrangements...
  2. ncbi request reprint PMX2B, a new candidate gene for Hirschsprung's disease
    H K Benailly
    Département de génétique, Hopital Necker Enfants Malades, Paris, France
    Clin Genet 64:204-9. 2003
    ..The present observation suggests that PMX2B haploinsuffciency might predispose to HSCR...
  3. ncbi request reprint Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis
    H Elghezal
    Service de Cytogénétique, Hopital Necker Enfants Malades, Paris, France
    Genes Chromosomes Cancer 30:383-92. 2001
    ....
  4. ncbi request reprint Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
    S Brisset
    Service de Cytogénétique et d Embryologie, Hopital Necker Enfants Malades, Paris, France
    Am J Med Genet 113:339-45. 2002
    ....
  5. ncbi request reprint [Microarray CGH: principle and use for constitutional disorders]
    D Sanlaville
    Service de Cytogénétique, Hopital Necker Enfants Malades, Assistance Publique Hopitaux de Paris, 149, rue de Sevres, 75015 Paris, France
    Arch Pediatr 12:1515-20. 2005
    ..Finally its is unlikely that it will make karyotyping obsolete as it does not allow to detect balanced rearrangements which after meiotic segregation might result in genome imbalance in the progeny...
  6. ncbi request reprint The TEL gene products: nuclear phosphoproteins with DNA binding properties
    H Poirel
    U 301 de l Institut National de la Santé et de la Recherche Médicale INSERM and SD 401 No 301 CNRS, Paris, France
    Oncogene 14:349-57. 1997
    ..In vivo, each of these primary translational products is modified by multiple phosphorylation events...
  7. ncbi request reprint A CGH study of 27 patients with CHARGE association
    D Sanlaville
    Département de Génétique Hôpital Necker Enfants Malades, Paris, France
    Clin Genet 61:135-8. 2002
    ..It is expected that more stringent diagnostic criteria of CHARGE association could define a more homogeneous group of patients where a single genetic cause might be identified...
  8. ncbi request reprint The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
    S P Romana
    U 301 de l Institut National de la Santé et de la Recherche Médicale INSERM, Paris, France
    Blood 85:3662-70. 1995
    ....
  9. ncbi request reprint NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance
    P Ballerini
    Leukemia 19:468-70. 2005
  10. ncbi request reprint [Spectral karyotyping (SKY) principle, avantages and limitations]
    M A Belaud-Rotureau
    Service d Histologie, Embryologie et Cytogenetique, Hopital Necker Enfants Malades, Paris
    Ann Biol Clin (Paris) 61:139-46. 2003
    ..Moreover, we present an easy way to build efficient sky probes with a best sensitivity than the probes classically used...
  11. ncbi request reprint Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report
    G Joly-Helas
    Laboratory of Cytogenetics, Rouen University Hospital, Rouen Cedex, France
    Hum Reprod 22:1292-7. 2007
    ..This particular case stresses the point of the relevance and feasibility of ICSI procedure in cases of balanced CCRs...
  12. ncbi request reprint Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocation
    G Soler
    Leukemia 22:1278-80. 2008
  13. ncbi request reprint Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene
    V Malan
    Clin Genet 73:89-91. 2008