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 *

120 related articles for article (PubMed ID: 903150)

  • 1. A case of 9p- syndrome.
    Kuroki Y; Yokota S; Nakai H; Yamamoto Y; Matsui I
    Hum Genet; 1977 Aug; 38(1):107-11. PubMed ID: 903150
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ; Hustinx TW; Dunk-Tillemans AA; Scheres JM; Tjon YS
    Ann Genet; 1978 Mar; 21(1):51-5. PubMed ID: 308344
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].
    Turleau C; De Grouchy J; Roubin M; Chavin-Colin F; Cachin O
    Ann Genet; 1975 Jun; 18(2):125-9. PubMed ID: 1081365
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome.
    Daniel A; Ekblom L; Phillips S; FitzGerald JM; Opitz JM
    Am J Med Genet; 1985 Nov; 22(3):577-84. PubMed ID: 4061490
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Partial monosomy 7q syndrome due to distal interstitial deletion.
    Stallard R; Juberg RC
    Hum Genet; 1981; 57(2):210-3. PubMed ID: 7228036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A 13-year-old girl with Wolf's syndrome and karyotype 46,XX,del(4)(pter integral p15::p12 integral qter),9qh+. Increased risk of structural chromosome abnormalities in the progeny of mothers with 9qh+.
    Nielsen J; Fischer O; Rasmussen K; Sillesen I; Bernsen A; Saldaña-Garcia P
    J Ment Defic Res; 1977 Jun; 21(2):119-26. PubMed ID: 894706
    [No Abstract]   [Full Text] [Related]  

  • 11. Trisomy for the distal half of the short arm of chromosome 9. A variant of the trisomy 9p syndrome.
    Lewandowski RC; Yunis JJ; Lehrke R; O'Leary J; Swaiman KF; Sanchez O
    Am J Dis Child; 1976 Jun; 130(6):663-7. PubMed ID: 937286
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ["Free" 9p trisomy in a male child with severe mental retardation (author's transl)].
    Aller V; Abrisqueta JA; Martín-Lucas MA; de Torres ML; del Mazo J; Pérez-Castillo A
    An Esp Pediatr; 1979 May; 12(5):463-8. PubMed ID: 464416
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion of the short arm of chromosome No. 10.
    Shokeir MH; Ray M; Hamerton JL; Bauder F; O'Brien H
    J Med Genet; 1975 Mar; 12(1):99-103. PubMed ID: 47396
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 9p-syndrome: two new observations.
    Szymańska J; Gutkowska A; Kubalska J; Krajewska-Walasek M; Wiśniewski L
    Klin Padiatr; 1984; 196(2):121. PubMed ID: 6737949
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 9p with an isochromosome of 9p.
    Smith G; McCaa A; Kelly TE
    Hum Genet; 1978 May; 42(1):93-7. PubMed ID: 649175
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Trisomy 9p : 2 further cases].
    Turleau C; de Grouchy J; Chavin-Colin F; Roubin M; Langmaid H
    Ann Genet; 1974 Sep; 17(3):167-74. PubMed ID: 4548817
    [No Abstract]   [Full Text] [Related]  

  • 18. Partial trisomy 9q-in a polymalformed new-born infant. Karyotype: 47,XX, + del (9) (q33).
    Fryns JP; Smeets E; Eggermont E; Delire C; Van den Berghe H
    Acta Paediatr Belg; 1978; 31(4):237-40. PubMed ID: 742362
    [No Abstract]   [Full Text] [Related]  

  • 19. Chromosome study of the family with a daughter showing 9p+ syndrome.
    Santadusit A; Wangpreedalertkul W; Anusri Y; Meevatee U
    J Med Assoc Thai; 1981 Sep; 64(9):480-4. PubMed ID: 7299300
    [No Abstract]   [Full Text] [Related]  

  • 20. Tetrasomy 9p: confirmation by enzyme analysis.
    Moedjono SJ; Crandall BF; Sparkes RS
    J Med Genet; 1980 Jun; 17(3):227-30. PubMed ID: 7401135
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.