BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 555637)

  • 21. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH; Martelli-Soares LR; Sarquis-Cintra T; Machado ML; Lison MP
    Ann Genet; 1990; 33(1):56-9. PubMed ID: 2195984
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Partial monosomy due to long-arm deletion of chromosome 11 : del (11) (q23) (author's transl)].
    Léonard C; Courpotin C; Labrune B; Lepercq G; Kachaner J; Caut P
    Ann Genet; 1979 Jun; 22(2):115-20. PubMed ID: 315201
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal.
    Fryns JP; Kleczkowska A; Casaer P; van den Berghe H
    Ann Genet; 1986; 29(1):49-52. PubMed ID: 3487277
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD; Hansen KL; Littlefield CA
    Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U
    Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M
    Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. Tetrasomy 9p caused by idic (9) (pter----q13----pter).
    Cavalcanti DP; Ferrari I; de Almeida JC; de Pina Neto JM; de Oliveira JA
    Am J Med Genet; 1987 Jul; 27(3):497-503. PubMed ID: 3631125
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.
    Alfi O; Donnell GN; Crandall BF; Derencsenyi A; Menon R
    Ann Genet; 1973 Mar; 16(1):17-22. PubMed ID: 4541805
    [No Abstract]   [Full Text] [Related]  

  • 31. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E; Piussan C; Risbourg B; Dutrillaux B
    Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J; Rethoré MO; Berger R; Abonyi D; Dutrillaux B; See G
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
    [No Abstract]   [Full Text] [Related]  

  • 33. Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).
    Hernandez A; Rivera H; Jiménez-Sainz M; Fragoso R; Nazara Z; Cantu JM
    Ann Genet; 1979; 22(3):155-7. PubMed ID: 316671
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The 9p--syndrome.
    Alfi OS; Donnell GN; Derencsenyi A
    Birth Defects Orig Artic Ser; 1976; 12(5):157-60. PubMed ID: 953217
    [No Abstract]   [Full Text] [Related]  

  • 35. [Partial monosomy 11q. A new case].
    Bresson JL; Noir A
    Ann Genet; 1977 Mar; 20(1):63-6. PubMed ID: 302678
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Trisomy 4p. A case presentation (author's transl)].
    Delgado A; Egüés J; Muñoz M; González Villa P; Bernaola E; del Amo A
    An Esp Pediatr; 1981 Oct; 15(4):383-9. PubMed ID: 7337304
    [No Abstract]   [Full Text] [Related]  

  • 37. [Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].
    Ayraud N; Rovinski J; Lambert JC; Galiana A
    Ann Genet; 1976 Dec; 19(4):265-8. PubMed ID: 797303
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.
    Hoo JJ; Fischer A; Fuhrmann W
    Ann Genet; 1982; 25(4):249-52. PubMed ID: 6985017
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE; Appadorai V; Breg WR; Howard RO
    Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
    [No Abstract]   [Full Text] [Related]  

  • 40. [Partial deletion of the short arm of the chromosome 9].
    Serville F; Allain D; Broustet A; Martin C; Gachet M; Babin JP; Cenraud J
    Ann Genet; 1976 Jun; 19(2):143. PubMed ID: 1085605
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.