BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 7035334)

  • 1. Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.
    Duckett DP; Roberts SH
    Hum Genet; 1981; 58(4):377-86. PubMed ID: 7035334
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
    Coco R; del Rey G
    J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11).
    Murthy DS; Patel ZM; Ambani LM
    Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS; Dosik H; Wexler IB
    J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocation.
    Armendares S; Salamanca-Gómez F
    Clin Genet; 1978 Jan; 13(1):17-24. PubMed ID: 624187
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
    Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Distal trisomy 14q caused by a paternal translocation (6;14)].
    Velasco F; Clusellas N; Godo RM; Antich J
    An Esp Pediatr; 1984 Nov; 21(7):681-7. PubMed ID: 6524780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.
    Rosi G; Venti G; Migliorini Brushelli G; Donti E; Bocchini V; Armellini R
    Hum Genet; 1979 Sep; 51(1):67-72. PubMed ID: 500094
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
    Komatsu H; Kihara A; Komura E; Mitsufuji N; Tsujii H; Kakita S; Ikuta H
    Genet Couns; 2001; 12(2):137-43. PubMed ID: 11491308
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation.
    Sekhon GS; Taysi K; Rath R
    Hum Genet; 1978 Oct; 44(1):99-103. PubMed ID: 711241
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents.
    Neu RL; Kousseff BG; Hardy DE; Essig YP; Miller KL; Jervis GA; Tedesco TA
    J Med Genet; 1988 Sep; 25(9):631-3. PubMed ID: 3184143
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.
    Stengel-Rutkowski S; Warkotsch A; Schimanek P; Stene J
    Clin Genet; 1984 Jun; 25(6):500-21. PubMed ID: 6539659
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Partial distal trisomy 13q resulting from familial reciprocal 5/13 translocation.
    Yanagisawa S; Yokoyama H; Agena N
    Hum Genet; 1978 Dec; 45(3):345-50. PubMed ID: 738734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.
    Duckett DP; Roberts SH; Davies P
    Hum Genet; 1984; 67(2):156-61. PubMed ID: 6336319
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
    Lindenbaum RH; Bobrow M
    J Med Genet; 1975 Mar; 12(1):29-43. PubMed ID: 123589
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)].
    Castel Y; Rivière D; Boycly JY; Toudic L
    Ann Genet; 1976 Mar; 19(1):15-9. PubMed ID: 1084116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.