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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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10q230

10q23
  • Barisic I, Zergollern L, Muzinic D, Hitrec V.: Risk estimates for balanced reciprocal translocation carriers - prenatal diagnosis experience. Clin. Genet. 49:145-151, 1996. [PubMed: 8737980]
    Family No. 27:
    t(10;11)(q23;q22)pat.,Fetal karyotype - 46,XY,t(10;11).
    Aberration: Reciprocal translocation
    Index Terms: Risk estimates
    Positive band
  • Same entry as in 04p130,09p230 (Boue and Gallano, 1984).

  • Boue A, Gallano P: A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses. Prenat. Diag. 4:45-67, 1984. [PubMed: 6463033]
    t(10;20)(q23;q13).
    Aberration: Reciprocal translocation
    Positive band
  • Farrell S A, Szymonowicz W, Chow G, Summers A M: Interstitial deletion of chromosome 10q23: a new case and review. J. Med. Genet. 30:248-250, 1993. [PMC free article: PMC1016310] [PubMed: 7682619]
    46,XY,del(10)(q22.3q23.2) or (q23.2q24.1)de novo.
    Aberration: Interstitial deletion
    Chromosomal Aneuploidy: 10q-
    Positive band
  • Ferguson-Smith M A, Page B M: "Pachytene analysis in a human reciprocal (10;11) translocation." J. Med. Genet. 10:282-287, 1973. [PMC free article: PMC1013034] [PubMed: 4774538]
    46,XY,t(10;11)(q23;q24).,46,XY,t(10;11)(10pter->10q23::11q24->11qter;,11pter->11q24::10q23->10qter).,MI,22,XY,IV(10;11) or MI,23,X,Y,IV(10;11).,46,XX,der(11)t(10;11)(q23;q24)pat.
    Aberration: Reciprocal translocation
    Positive band
  • Hamerton J L, Canning N, Ray M, Smith S: A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clin. Genet. 8:223-243, 1975. [PubMed: 1183067]
    46,XY,t(10;12)(q23;q13).
    Case 8252 (200272) in this report.
    46,XY,der(10)der(12)t(10;12)(q23;q13)pat.
    Aberration: Simple translocation
    Positive band
  • Hsu L Y F, Yu M T, Richkind K E, Van Dyke D L, Crandall B F, Saxe D F, Khodr G S, Mennuti M, Stetten G, Miller W A, Priest J H.: Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study. Prenat. Diag. 16: 1-28, 1996. [PubMed: 8821848]
    Case IV-8 from Richkind K E (9100399).
    mos46,XX/46,XX,del(10)(q23)[14.7%].
    Normal female liveborn.
    Aberration: Terminal deletion
    Chromosomal Aneuploidy: 10q-
    Positive band
  • Maltby E L, Higgins S: Folate sensitive site at 10q23 and its expression as a deletion. J. Med. Genet. 24:299, 1987. [PMC free article: PMC1050055] [PubMed: 3585944]
    Aberration: Fragile sites
    Positive band
  • Samadder P, Evans J A, Chudley A E: Segregation analysis of rare autosomal folate sensitive sites. AJMG 46:165-171, 1993. [PubMed: 8484403]
    The authors found a deficiency of offspring expressing fragile sites when transmission was through fathers, suggesting gametic selection or the phenomenon of parental genomic imprinting.
    Aberration: Fragile sites
    Positive band
  • Sutherland G R, Baker E G, Mulley J C: Genetic length of a human chromosomal segment measured by recombination between two fragile sites. Science 217:373-374, 1982. [PubMed: 7089572]
    The genetic length of chromosome between the fragile sites was 11 female centimorgans within a 95% probability interval of 4 to 28 centimorgans.
    Aberration: Fragile sites
    Positive band
  • Zaslav A L, Fox J E, Jacob J, Kazi R, Allan S, Shklooskaya T, Sohal D, Kleyman S M, Verma R S.: Significance of a prenatally diagnosed del(10)(q23). AJMG DOI=10.1002/ajmg.10112:107:174-176, 2002. [PubMed: 11807894]
    Prenatal=mos46,XY[45]/46,XY,del(10)(q23)[9].,Postnatal blood=mos46,XY[200]/46,XY,fra or del(10(q23)[3].,Placenta (postnatal)=46,XY.,Mother=46,XX[188]/46,XX,fra(10)(q23)[8].
    The family was of East Indian origin. The child was developing normally.
    The deletion originated from a fragile site at 10q23.
    Aberration: TD,FS
    Chromosomal Aneuploidy: 10q-
Copyright © 2011-2013, Digamber Borgaonkar.
Bookshelf ID: NBK105815

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