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 *

140 related articles for article (PubMed ID: 2614798)

  • 1. Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation.
    Pinto MR; Leite RP; Areias A
    J Med Genet; 1989 Dec; 26(12):778-80. PubMed ID: 2614798
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Features of Turner's and DiGeorge's syndromes with X;22 translocation.
    Gilgenkrantz S; Teboul M
    J Med Genet; 1990 Dec; 27(12):791. PubMed ID: 2095774
    [No Abstract]   [Full Text] [Related]  

  • 3. A deletion in chromosome 22 can cause DiGeorge syndrome.
    de la Chapelle A; Herva R; Koivisto M; Aula P
    Hum Genet; 1981; 57(3):253-6. PubMed ID: 7250965
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).
    Faed MJ; Robertson J; Beck JS; Cater JI; Bose B; Madlom MM
    J Med Genet; 1987 Apr; 24(4):225-7. PubMed ID: 3585938
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome.
    Schwanitz G; Zerres K
    Ann Genet; 1987; 30(2):80-4. PubMed ID: 3314667
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DiGeorge syndrome and 22q11 rearrangements.
    Augusseau S; Jouk S; Jalbert P; Prieur M
    Hum Genet; 1986 Oct; 74(2):206. PubMed ID: 3770751
    [No Abstract]   [Full Text] [Related]  

  • 7. Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature.
    Dallapiccola B; Marino B; Giannotti A; Valorani G
    Ann Genet; 1989; 32(2):92-6. PubMed ID: 2667458
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of incomplete DiGeorge syndrome associated with partial monosomy 22q11.1 due to maternal 14;22 translocation.
    Nukina S; Nishimura Y; Kinugasa A; Sawada T; Hamaoka K; Inazawa J; Tsuda S; Abe T
    Jinrui Idengaku Zasshi; 1989 Sep; 34(3):235-41. PubMed ID: 2634137
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DiGeorge syndrome in a child with partial monosomy of chromosome 22.
    Annerén G; Gustafsson J; SunnegÄrdh J
    Ups J Med Sci; 1989; 94(1):47-53. PubMed ID: 2711536
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X/X translocation and Turner's syndrome in a woman with climacterium praecox.
    Nielsen J; Kristoffersen E; Homma A
    Acta Obstet Gynecol Scand; 1979; 58(3):309-12. PubMed ID: 484225
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence.
    Mascarello JT; Bastian JF; Jones MC
    Am J Med Genet; 1989 Jan; 32(1):112-4. PubMed ID: 2705472
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Monosomy 22pter-22q11.2 with monosomy 10q26.2-10qter without Di George syndrome].
    Arslanian A; Veneziano G; Grasso M; Brugo A; Bertamino F
    Pathologica; 1985; 77(1052):767-70. PubMed ID: 3842998
    [No Abstract]   [Full Text] [Related]  

  • 13. Familial DiGeorge syndrome and associated partial monosomy of chromosome 22.
    Greenberg F; Crowder WE; Paschall V; Colon-Linares J; Lubianski B; Ledbetter DH
    Hum Genet; 1984; 65(4):317-9. PubMed ID: 6693120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Severe eczema in a patient with DiGeorge's syndrome.
    Archer E; Chuang TY; Hong R
    Cutis; 1990 Jun; 45(6):455-9. PubMed ID: 2350983
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
    Greenberg F; Elder FF; Haffner P; Northrup H; Ledbetter DH
    Am J Hum Genet; 1988 Nov; 43(5):605-11. PubMed ID: 3189331
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X;Y translocation in a female with streak gonads, H-Y- phenotype, and some features of Turner's syndrome.
    Kelly TE; Wachtel SS; Cahill L; Barnabei VM; Willson-Suddath K; Wyandt HE
    Cytogenet Cell Genet; 1984; 38(2):122-6. PubMed ID: 6467986
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A synovial sarcoma with t(X;18)(p11;q11) in a patient with Turner's syndrome.
    Miozzo M; Sozzi G; Cariani CT; Di Palma S; Luksch R; Azzarelli A; Pierotti MA; Della Porta G
    Genes Chromosomes Cancer; 1992 Mar; 4(2):192-3. PubMed ID: 1373322
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
    Bjerglund Nielsen L; Nielsen IM
    Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Thymic hypoplasia (DiGeorge's syndrome).
    Berman BA; Ross RN
    Cutis; 1984 Mar; 33(3):248, 253, 262. PubMed ID: 6723361
    [No Abstract]   [Full Text] [Related]  

  • 20. Temporal bone pathology in DiGeorge's syndrome.
    Ohtani I; Schuknecht HF
    Ann Otol Rhinol Laryngol; 1984; 93(3 Pt 1):220-4. PubMed ID: 6732106
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.