BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 6985017)

  • 21. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
    Repetto GM; Wagstaff J; Korf BR; Knoll JH
    Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Trisomy 9p: a clinical picture and the importance of examining the family].
    van Ravenswaaij-Arts C; van der Looij E; Smeets D
    Ned Tijdschr Geneeskd; 1999 Mar; 143(13):682-6. PubMed ID: 10321302
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal morphology of partial monosomy 18q.
    Lazjuk G; Zolotukhina T; Kirillova I; Lurie I; Novikova I; Abasheva G
    Zentralbl Gynakol; 1987; 109(2):126-9. PubMed ID: 3577468
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C; Crippa L; Delozier C; Michail E; Graber P
    J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The 9p trisomy syndrome due to inherited translocation.
    Weber F; Muller H; Sparkes R
    Birth Defects Orig Artic Ser; 1975; 11(5):201-5. PubMed ID: 1218214
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. The 9p- syndrome.
    Alfi OS; Donnell GN; Allderdice PW; Derencsenyi A
    Ann Genet; 1976 Mar; 19(1):11-6. PubMed ID: 1084115
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C; Bouquier JJ; Ronayette D; Tchertoff C; Faugeras C; Barthe D; Laleu J
    Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
    [No Abstract]   [Full Text] [Related]  

  • 31. Interchromosomal duplication for the short arm of chromosome no. 9: report of three cases due to a familial translocation t(9; 11) and one case with a de novo 47, XX, +9p karyotype.
    Lin CC; Holman G; Sewell L; Bowen P; Biederman B
    J Ment Defic Res; 1977 Dec; 21(4):309-29. PubMed ID: 604504
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V
    Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract]   [Full Text] [Related]  

  • 33. A clinical syndrome associated with 5p duplication and 9p deletion.
    Liberfarb RM; Atkins L; Holmes LB
    Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF; Shear CS; Jalowayski I; Akesson HO
    J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
    [No Abstract]   [Full Text] [Related]  

  • 35. Concordant congenital malformations in twins with inherited translocation: t(9p--;13q+).
    Sekhon GS; Taysi K
    Hum Genet; 1979 Sep; 50(3):271-6. PubMed ID: 489011
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trisomy 9p with i(9p) and t(9q18p).
    Herva R; Koivisto M
    Hum Genet; 1979 Sep; 50(3):237-40. PubMed ID: 489006
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Different risks in two familial translocations t(9;12) with similar breakpoints.
    Midro AT; Stengel-Rutkowski S; Krajewska-Walasek M; Szymańska J; Lassota M; Lesniewicz R; Jaworowska B
    Ann Genet; 1992; 35(1):33-40. PubMed ID: 1610118
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46,XY, -9, +DER(9)T(6:9)(p211:p24).
    Eden MS; Thelin JW; Michalski K; Mitchell JA
    Clin Genet; 1985 Nov; 28(5):375-84. PubMed ID: 4085142
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome.
    Hoo JJ; Parslow MI; Shaw RL; Veale AM
    Clin Genet; 1979 Sep; 16(3):151-5. PubMed ID: 487636
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
    Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.