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 *

154 related articles for article (PubMed ID: 6846396)

  • 1. Origin of a paternal (13q;15q) translocation leading to dup(13q) in two half sibs.
    De los Cobos LF
    Am J Med Genet; 1983 Apr; 14(4):617-23. PubMed ID: 6846396
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial t(4;13) with abnormal offspring in three generations.
    Najafzadeh TM; Littman VA; Dumars KW
    Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
    Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication of distal 15q: report of five new cases from two different translocation kindreds.
    Lacro RV; Jones KL; Mascarello JT; Jones OW; Wilson N; Jones MC
    Am J Med Genet; 1987 Mar; 26(3):719-28. PubMed ID: 3565485
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
    Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brief cytogenetic report on maternal translocation t(7;9) (p22:p13): two sibs with duplication 9p and one sib with the balanced translocation.
    Wajntal A; Gonzalez CH; Koiffmann CP; de Souza DH
    Am J Med Genet; 1985 Feb; 20(2):265-9. PubMed ID: 3976719
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brief clinical report: duplication of distal 17q: report of an observation.
    Naccache NF; Vianna-Morgante AM; Richieri-Costa A
    Am J Med Genet; 1984 Mar; 17(3):633-9. PubMed ID: 6711615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].
    de Grouchy J; Turleau C; Danis F; Kohout G; Briard ML
    Ann Genet; 1978 Dec; 21(4):247-51. PubMed ID: 314266
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation.
    Chase TR; Jalal SM; Martsolf JT; Wasdahl WA
    Am J Med Genet; 1983 Feb; 14(2):347-51. PubMed ID: 6837629
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical diagnosis of partial duplication 7q.
    Bartsch O; Kalbe U; Ngo TK; Lettau R; Schwinger E
    Am J Med Genet; 1990 Oct; 37(2):254-7. PubMed ID: 2248294
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
    Badalian LO; Malygina NA; Gozman TV; Petrukhin AS; Mutovin GR
    Tsitol Genet; 1982; 16(2):17-21. PubMed ID: 7101445
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M; Stembalska A; Schlade K; Zych M
    Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
    Gonzalez CH; Billerbeck AE; Takayama LC; Wajntal A
    Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.