11p110

11p11

Publication Details

  • Aiello V, Ricci N, Palazzi P, D''Agostino G, Azzini G, Calzolari E: New variant of chromosome 11. AJMG 50:294-295, 1994. [PubMed: 8042675]
    An additional C-band positive region is identified in a man whose wife had pregnancy losses.
    Aberration: Marker chromosome
    No band

  • Autio-Harmainen H, de la Chapelle A: High resolution of a small pericentric inversion of chromosome 11. J. Med. Genet. 17:44-47, 1980. [PMC free article: PMC1048487] [PubMed: 7365763]
    de la Chapelle A, Simola K, Karli P, Lindenbaum R H, Robson E B, Cook P J L, Buckton K E: Linkage data on chromosome 11. Cytogenet. Cell Genet. 22:472-473, 1978. [PubMed: 752524]
    46,XX,inv(11)(p11q133)mat.,Proband was a 24 year old female, with 9 sibs, 7 were karyotyped, 5 were normal, and 2 were inversion heterozygotes.
    Aberration: Inversion pericentric
    No band

  • 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. 32:
    t(11;17)(p11;p13)pat.,Fetal karyotype - 46,XX,t(11;17).
    Family ascertained because of a previous infant with MCA.
    Aberration: Reciprocal translocation
    Index Terms: Risk estimates
    No band

  • 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]
    Casalone R, Fraccaro M, Francesconi D, Pasquali F, Poloni L, Zuffardi O, Bellomi A, Crosti N, Lo Monaco G B, Patriarca P L, Serventi M: Five unusual karyotypes in Down''s syndrome. Ann. Genet. 22:17-20, 1979.
    46,XY,t(11;21)(p11;q22).,46,XY,der(11)der(21)t(11;21)(p11;q22)pat.,t(11;12)(p11;q13).
    Case 5 in this report.
    47,XX,+21,der(11)der(21)t(11;21)(11qter->11p11::21q22->21qter;21pter->21q22::11p11->11pter).
    Aberration: Reciprocal translocation
    Index Terms: Down syndrome (Trisomy 21)
    No band

  • Chaabouni H, Chaabouni M, Maazoul F, M''Rad R, Jemma L B, Smaoui N, Terras K, Kammoun H, Belghith N, Ridene H, Oueslati B, Zouari F.: Prenatal diagnosis of chromosome disorders in Tunisian population. Ann. Genet. 44:99-104, 2001. [PubMed: 11522249]
    46,XY,t(11;22)(p11;p12).
    Aberration: Simple translocation
    Index Terms: Tunisian

  • de Martinville B, Giacalone J, Shin C, Weinberg R A, Francke U: Oncogene from human EJ bladder carcinoma is located on the short arm of chromosome 11. Science 219:498-501, 1983. [PubMed: 6297001]
    t(11;15)(p11;p12).
    Index Terms: Oncogene
    No band

  • Fryns J P, Haspeslagh M, Goddeeris P, van Aerde J, Eggermont E, van den Berghe H: Balanced and unbalanced pericentric inversion of chromosome 11. Ann. Genet. 24:182-183, 1981. [PubMed: 6974533]
    Fryns J P, Kleczkowska A, Vandenberghe K, Moerman F, Van den Berghe H: Cystic hygroma and hydrops fetalis in dup(11p) syndrome. AJMG 22:287-289, 1985. [PubMed: 4050859]
    Patient M. K. died 6 hours after birth due to malformations.
    46,XY,inv(11)(p11q25).&46,XX,rec(11)dup p,inv(11)(p11q25).
    Aberration: Inversion pericentric
    Index Terms: Cystic hygroma,Hydrops,Hygromata
    No band

  • Heideman R L, McGavran L, Waldstein G: Nephroblastomatosis and deletion of 11p. The potential etiologic relationship to subsequent Wilm''s tumor. Am. J. Ped. Hemat./Oncol. 8:231-234, 1986. [PubMed: 3021014]
    Patient was 11 months old. Cells from the nodule of renal blastoma showed the deletion, whereas blood and fibroblasts were normal.
    46,XY,del(11)(p11p14.3).
    Aberration: Interstitial deletion
    MIM#: 194070
    Index Terms: Wilms tumor
    No band

  • Higgins J V, Center J, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]
    Observation No. 936.
    46,XY,t(11;12)(p11;q15)mat.
    Aberration: Reciprocal translocation
    No band

  • Larsen J W, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]
    Observation No. 950.
    47,XY,t(11;16)(p11;q11)mat,+21.
    Aberration: Reciprocal translocation
    No band

  • Mann J, Wcislo K, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]
    Observation No. 942.
    46,XY,t(11;14)(p11;q11)mat.
    Aberration: Reciprocal translocation
    No band

  • Ohnishi Y, Shigeto M, Ishibashi T, Hirata J: Familial pericentric inversion of chromosome 11 in a child with sporadic unilateral retinoblastoma. Ophthal. Paed. Genet. 11:281-285, 1990. [PubMed: 2096356]
    46,XY,inv(11)(p11q23)pat.
    The patient was 12 months old.
    Aberration: Inversion pericentric
    Index Terms: Retinoblastoma
    No band

  • Portnoi M F, Joye N, Van den Akker J, Morlier G, Taillemite J L: Karyotypes of 1142 couples with recurrent abortion. Obst. Gynecol. 72:31-34, 1988. [PubMed: 3242501]
    46,XX,t(11;22)(p11;q13).
    Aberration: Reciprocal translocation
    No band

  • Richkind K E, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]
    Observation No. 1307.
    46,XY,inv(11)(p11q13.1)pat.
    Aberration: Inversion pericentric
    No band

  • Schmutz S M: Deletion of chromosome 11 (p11p13) in a patient with Beckwith-Wiedemann syndrome. Clin. Genet. 30:154-156, 1986. [PubMed: 3780031]
    Patient was 6 months old.
    46,XX,del(11)(p11p13)de novo.
    Aberration: Interstitial deletion
    MIM#: 130650
    Index Terms: Beckwith-Wiedemann syndrome
    No band

  • Simola K, Karli P, de la Chapelle A: Two pericentric inversions of human chromosome 11. J. Med. Genet. 14:371-374, 1977. [PMC free article: PMC1013623] [PubMed: 592354]
    inv(11)(p11q11) occurred in 9 members of 3 generations. There was no clear-cut evidence of any clinical consequence.
    Aberration: Inversion pericentric
    No band

  • Stoll C: Cytogenetic findings in 122 couples with recurrent abortions. Hum. Genet. 57:101-103, 1981. [PubMed: 7262863]
    Case 4:46,XX,t(11;22)(p11;p11).
    Aberration: Simple translocation
    Index Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)
    No band

  • Tomkins D J: "Unstable familial translocations: A t(11;22)mat inherited as a t(11;15)." AJHG 33:745-751, 1981. [PMC free article: PMC1685141] [PubMed: 7294023]
    Mother: 46,XX,t(11;22)(p11;p12).,46,XX,der(11)der(22)t(11;22)(p11;p12).,Proband: 46,XX,t(11;15)(p11;p12).,Proband was karyotyped because of history of drug use prior to her marriage. Between her mother, her sister and herself there have been 7 miscarriages and one stillbirth.
    Aberration: Unstable translocation
    Index Terms: Stillborn (premature)
    No band

  • Warburton D: De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. AJHG 49:995-1013, 1991. [PMC free article: PMC1683246] [PubMed: 1928105]
    46,XY,t(11;15)(p11;q11).
    Aberration: Reciprocal translocation
    No band