These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 422200)

  • 1. A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.
    Simoni G; Montali E; Rossella F; Dalprà L; Lo Curto F
    Hum Genet; 1979 Jan; 46(2):159-62. PubMed ID: 422200
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13).
    Ventruto V; Pisciotta R; Renda S; Festa B; Rinaldi MM; Stabile M; Cavaliere ML; Esposito M
    Am J Med Genet; 1983 Dec; 16(4):589-94. PubMed ID: 6660251
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK; Wilroy RS; Summitt JB; Tucker B; Herrod HG; Tharapel AT
    Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo translocation heterozygote with three reciprocal translocations.
    Watt JL; Couzin DA
    J Med Genet; 1983 Oct; 20(5):385-8. PubMed ID: 6644769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R; Gross-Kieselstein E; Hurvitz H; Dagan J; Kerem E; Zlotogora J
    J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dup(3)(p2----pter) in two families, including one infant with cyclopia.
    Gimelli G; Cuoco C; Lituania M; Cordone M; Aricò M; Bianchi E; Maraschio P; Zuffardi O
    Am J Med Genet; 1985 Feb; 20(2):341-8. PubMed ID: 3919583
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocations.
    Stoll C; Flori E; Macler J; Renaud R
    Hum Genet; 1979 Mar; 47(2):221-4. PubMed ID: 437789
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
    Dufke A; Mayrhofer H; Enders H; Kaiser P; Leipoldt M
    Cytogenet Cell Genet; 2001; 93(3-4):168-70. PubMed ID: 11528107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo translocation involving chromosomes 2, 8, and 20.
    Zaletajev DV; Marincheva GS; Tsvetkova TG
    J Med Genet; 1984 Jun; 21(3):231. PubMed ID: 6748024
    [No Abstract]   [Full Text] [Related]  

  • 10. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families.
    Prieto F; Badia L; Asensi F; Roques V
    Hum Genet; 1980; 54(1):7-11. PubMed ID: 7390483
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A de novo translocation in a family with a balanced reciprocal chromosomal translocation.
    Short MP; Gilbert F; Hirschhorn K
    Clin Genet; 1986 Feb; 29(2):143-6. PubMed ID: 3955864
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two reciprocal translocations associated with microcephaly and retardation.
    Bell EF; Warburton D
    J Med Genet; 1977 Apr; 14(2):141-2. PubMed ID: 853319
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
    Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
    BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome abnormalities in 118 couples with recurrent spontaneous abortions.
    Tóth A; Gaál M; Bösze P; László J
    Gynecol Obstet Invest; 1984; 18(2):72-7. PubMed ID: 6479698
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complex chromosome rearrangements. Report of a new case and literature review.
    Pai GS; Thomas GH; Mahoney W; Migeon BR
    Clin Genet; 1980 Dec; 18(6):436-44. PubMed ID: 7449183
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome 6/15 translocation with multiple congenital anomalies.
    Ming PM; Goodner DM; Park TS
    Obstet Gynecol; 1977 Feb; 49(2):251-3. PubMed ID: 834413
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.
    Migliorini AM; Coco R; De Negrotti TC; Sanchez JM; Castineyra G
    J Med Genet; 1981 Oct; 18(5):383-5. PubMed ID: 6460105
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chronic myelogenous leukemia with translocations (3q-;9q+) and (17q-;22q+). Possible crucial cytogenetic events in the genesis of CML.
    Oshimura M; Ohyashiki K; Vehara M; Miyasaka Y; Osamura S; Tonomura A
    Hum Genet; 1981; 57(1):48-51. PubMed ID: 6943121
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Translocations involving chromosome 12. I. A report of a 12,21 translocation in a woman with recurrent abortions, and a study of the breakpoints and modes of ascertainment of translocations involving chromosome 12.
    Ford JH; Rofe RH; Pavy RP
    Hum Genet; 1981; 58(2):144-8. PubMed ID: 7286999
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mentally retarded child with a translocation involving chromosomes 12 and 19.
    Histinx TW; Gabreëls FJ; Rutten FJ; Korten II; Scheres JM; Joosten EM
    J Med Genet; 1975 Jun; 12(2):207-10. PubMed ID: 1142383
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.