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Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.

Cover of Chromosomal Variation in Man

Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].

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09p111

9p11.1
  • Same entry as in 47,XXY (Liehr et al, 2005).

  • Kraker W J, Borell T J, Schad C R, Pennington M J, Karnes P S, Dewald G W, Jenkins R B: Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocations. Mayo Clin. Proc. 67:658-662, 1992. [PubMed: 1434900]
    Case 1:
    46,XX,der(18)t(9;18)(p11.1;p11.1)mat.
    The patient was a newborn with MCA.
    Aberration: Simple translocation
    Chromosomal Aneuploidy: 9p+
    Index Terms: FISH
    Variable band
  • Tuerlings J H A M, de France H F, Hamers A, Hordijk R, Van Hemel J O, Hansson K, Hoovers J M N, Madan K, Van Der Blij-Philipsen M, Gerssen-Schoorl K B J, Kremer J A M, Smeets D F C M.: Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. Europ. J. Hum. Genet. 6:194-200, 1998. [PubMed: 9781022]
    46,XY,der t(9;22)(p11.1;p11.1)
    Aberration: Simple translocation
    Index Terms: ICSI
Copyright © 2011-2013, Digamber Borgaonkar.
Bookshelf ID: NBK106208
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