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Journal Abstract Search

247 related items for PubMed ID: 3879156

  • 1. 46,XX,-12,+der(12),rcp(3;12)(p25.1;p13.31)pat karyotype in a girl. Probable subregional assignment of glyceraldehyde-3-phosphate dehydrogenase locus to 12p13.1----p13.31 by exclusion mapping.
    Rivas F, Vaca G, Zúñiga G, González RM, Ruiz C, Rivera H, Moller M, Cantu JM.
    Ann Genet; 1985; 28(3):189-92. PubMed ID: 3879156
    [Abstract] [Full Text] [Related]

  • 2. Inherited partial trisomy 2: 46,XX,1p+;t(1;2) (p36;q31).
    Warren RJ, Panizales EG, Cantwell RJ.
    Birth Defects Orig Artic Ser; 1975; 11(5):177-9. PubMed ID: 1218210
    [No Abstract] [Full Text] [Related]

  • 3. [Effect of gene dosage on the glyceraldehyde-3-phosphate dehydrogenase enzyme (GAPD) in partial 12p13.3 pter trisomy].
    Barros-Núñez P, Vaca G, Sánchez-Corona J, Zúñiga G, Medina C, Rivas F, Rodríguez RM, Moller M, García-Cruz D.
    Bol Med Hosp Infant Mex; 1990 Sep; 47(9):656-9. PubMed ID: 2271129
    [Abstract] [Full Text] [Related]

  • 4. 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 Sep; 28(3):193-6. PubMed ID: 3879157
    [Abstract] [Full Text] [Related]

  • 5. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
    Ottolina de Bracamonte N, Velazco JQ, Hammond Figueroa FG.
    Acta Cient Venez; 1982 Sep; 33(4):342-7. PubMed ID: 7186725
    [No Abstract] [Full Text] [Related]

  • 6. Autosomal syndromes.
    Summitt RL.
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract] [Full Text] [Related]

  • 7. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS, Summitt RL, Martens P, Gooch WM.
    Ann Genet; 1977 Dec; 20(4):237-42. PubMed ID: 305749
    [Abstract] [Full Text] [Related]

  • 8. [Partial 7q trisomy].
    Serville F, Broustet A, Sandler B, Bourdeau MJ, Leloup M.
    Ann Genet; 1975 Mar; 18(1):67-70. PubMed ID: 1080040
    [Abstract] [Full Text] [Related]

  • 9. [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 15; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract] [Full Text] [Related]

  • 10. [Partial trisomy for the distal part of the short arm of chromosome 11 due to paternal translocations 11/5].
    Bajolle F, Rullier J, Picard AM, Legrele G.
    Ann Genet; 1978 Sep 15; 21(3):181-5. PubMed ID: 315195
    [Abstract] [Full Text] [Related]

  • 11. [12 p trisomy. A new case (author's transl)].
    Kubryk N, Prieur M, Borde M.
    Ann Pediatr (Paris); 1980 Dec 15; 27(10):695-9. PubMed ID: 7212558
    [No Abstract] [Full Text] [Related]

  • 12. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
    Siffroi JP, Romani F, Viguié F, Lejeune C.
    Ann Genet; 1984 Dec 15; 27(4):241-4. PubMed ID: 6335372
    [Abstract] [Full Text] [Related]

  • 13. 12P trisomy: a syndrome?
    Hoo JJ.
    Ann Genet; 1976 Dec 15; 19(4):261-3. PubMed ID: 1087857
    [Abstract] [Full Text] [Related]

  • 14. [46,XX,trcp(1;10),trcp(2;8) karyotype of maternal origin and 2p trisomy].
    Vianello MG, Fasce L, Besio B, Lupi M, Scribanis R, Sburlati C, Buoncompagni A.
    Minerva Pediatr; 1988 Sep 15; 40(9):561-9. PubMed ID: 3068505
    [No Abstract] [Full Text] [Related]

  • 15. Duplication 8p syndrome: studies in a family with a reciprocal translocation between chromosomes 8 and 12.
    Moreno Fuenmayor HM, Meilinger KL, Rucknagel DL, Mohrenweiser HL, Chu EH.
    Am J Med Genet; 1980 Sep 15; 7(3):361-8. PubMed ID: 7468661
    [Abstract] [Full Text] [Related]

  • 16. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
    Cantu JM, Salamanca F, Buentello L, Carnevale A, Armendares S.
    Ann Genet; 1975 Mar 15; 18(1):5-11. PubMed ID: 1080038
    [Abstract] [Full Text] [Related]

  • 17. Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1990 Mar 15; 33(1):43-5. PubMed ID: 2195980
    [Abstract] [Full Text] [Related]

  • 18. Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.
    Tenconi R, Baccichetti C, Anglani F, Pellergrino PA, Kaplan JC, Junien C.
    Ann Genet; 1975 Jun 15; 18(2):95-8. PubMed ID: 1081371
    [Abstract] [Full Text] [Related]

  • 19. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G.
    Genet Couns; 1999 Jun 15; 10(4):351-8. PubMed ID: 10631922
    [Abstract] [Full Text] [Related]

  • 20. [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].
    Morić-Petrović S, Laća Z, Krajgher A, Milośevic J.
    Ann Genet; 1976 Sep 15; 19(3):195-7. PubMed ID: 1086628
    [Abstract] [Full Text] [Related]

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