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 *

136 related articles for article (PubMed ID: 738724)

  • 1. Partial trisomy 2q and familial translocation t(2;18)(q31;p11).
    Wisniewski L; Chan R; Higgins JV
    Hum Genet; 1978 Dec; 45(2):225-8. PubMed ID: 738724
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 2q and familial translocation t(2;12)(q31;q24).
    Zabel B; Hansen S; Hartmann W
    Hum Genet; 1976 Apr; 32(1):101-4. PubMed ID: 1262021
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetics of partial trisomies. I. Trisomy 2q].
    Lur'e IV; Rumiantseva NV; Podleshchuk LV; Kaurov BA; Zaletaev DV
    Genetika; 1986 Jun; 22(6):1033-9. PubMed ID: 3732802
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.
    Zankl M; Schwanitz G; Schmid P; Zankl H; Dockter G; Rodewald A; Zang KD; Grosse KP
    Am J Med Genet; 1979; 4(1):5-16. PubMed ID: 495653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple cases of trisomy 9p/distal monosomy 18p in a family due to inherited translocation t (9:18).
    Valkova G; Grozdanova I; Shishkoval N; Hadzhipanayotova N
    Folia Med (Plovdiv); 1993; 35(3-4):27-34. PubMed ID: 7927051
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 'Pure' partial trisomy 2q in a male owing to malsegregation of a maternal translocation t(X;2)(p22.3;q32.1).
    Plessis G; Couturier J; Turleau C; Despoisses S; Delavenne J
    J Med Genet; 1985 Feb; 22(1):70-3. PubMed ID: 3981584
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Familial translocation 2; 17 with partial trisomy 2q32 to 2qter].
    Tancredi F; Ventruto V
    Pediatria (Napoli); 1981 Mar; 89(1):35-40. PubMed ID: 7290826
    [No Abstract]   [Full Text] [Related]  

  • 8. Monosomy 18p and pure trisomy 18p in a family with translocation (7;18).
    Habedank M; Trost-Brinkhues G
    J Med Genet; 1983 Oct; 20(5):377-9. PubMed ID: 6644768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23).
    Shawe DJ; Fear C; Appleyard WJ
    J Med Genet; 1983 Oct; 20(5):383-5. PubMed ID: 6196484
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial chromosome translocation t(3;18)(p21;p11).
    Buchinger G; Wettstein A; Metze H
    J Med Genet; 1981 Apr; 18(2):119-23. PubMed ID: 7241529
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
    Rosenmann A; Isacson M; Cohen R; Segal M; Cohen MM
    Ann Genet; 1978 Mar; 21(1):60-4. PubMed ID: 308346
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial trisomy 9q resulting from a familial translocation t(9;16)(q32;q24).
    Soltan HC; Jung JH; Pyatt Z; Singh RP
    Clin Genet; 1984 May; 25(5):449-54. PubMed ID: 6723106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Five familial cases with a trisomy 16p syndrome due to translocation.
    Leschot NJ; De Nef JJ; Geraedts JP; Becker-Bloemkolk MJ; Talma A; Bijlsma JB; Verjaal M
    Clin Genet; 1979 Sep; 16(3):205-14. PubMed ID: 487639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
    Siffroi JP; Romani F; Viguié F; Lejeune C
    Ann Genet; 1984; 27(4):241-4. PubMed ID: 6335372
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
    Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H
    Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 18. Trisomy 12p due to an adjacent 1 segregation of a maternal reciprocal translocation t(12;18) (p11;q23).
    Tenconi R; Giorgi PL; Tarantino E; Formica A
    Ann Genet; 1978 Dec; 21(4):229-33. PubMed ID: 314261
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings.
    Beneck D; Greco MA; Wolman SR; McMorrow LE; Jansen V; Cason J
    J Med Genet; 1986 Jun; 23(3):260-3. PubMed ID: 3723557
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy 12q associated with a familial translocation.
    Hemming L; Brown R
    Clin Genet; 1979 Jul; 16(1):25-8. PubMed ID: 477011
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.