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Journal Abstract Search

118 related items for PubMed ID: 3379382

  • 1. [A difficult cytogenetic diagnosis of 4p monosomy].
    Vittu G, Croquette MF, Boidein F, Cousin J.
    J Genet Hum; 1988 Jan; 36(1-2):75-82. PubMed ID: 3379382
    [Abstract] [Full Text] [Related]

  • 2. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
    Al-Awadi SA, Teebi AS, Sundareshan TS.
    Ann Genet; 1985 Jan; 28(3):181-4. PubMed ID: 3879154
    [Abstract] [Full Text] [Related]

  • 3. [Monosomy r(13). Report of a new case].
    Cuadrado Martín M, Boldova Aguar C, Carrasco Lorente S, Martínez Laborda S, López-Pisón J, Baldellou Vázquez A, Labarta Aizpún J, Marco Tello A, Rebage Moisés V.
    An Esp Pediatr; 2000 Dec; 53(6):592-5. PubMed ID: 11148159
    [Abstract] [Full Text] [Related]

  • 4. The 8p-syndrome.
    Ostergaard GZ, Tommerup N.
    Ann Genet; 1989 Dec; 32(2):87-91. PubMed ID: 2667457
    [Abstract] [Full Text] [Related]

  • 5. [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; 40(9):561-9. PubMed ID: 3068505
    [No Abstract] [Full Text] [Related]

  • 6. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
    Doco-Fenzy M, Elchardus JF, Brami G, Digeon B, Gruson N, Adnet JJ.
    Genet Couns; 1994 Sep; 5(1):39-44. PubMed ID: 8031534
    [Abstract] [Full Text] [Related]

  • 7. Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay: a 4p deletion?
    de Die-Smulders C, Schrander-Stumpel C, Fryns JP.
    Am J Med Genet; 1993 Nov 01; 47(6):936. PubMed ID: 7506486
    [No Abstract] [Full Text] [Related]

  • 8. Severe midline fusion defects in a newborn with 10q26----qter deletion.
    Fryns JP, Kleczkowska A, Fivez H, Van den Berghe H.
    Ann Genet; 1989 Nov 01; 32(2):124-5. PubMed ID: 2757362
    [Abstract] [Full Text] [Related]

  • 9. De novo inverted interstitial ("mirror") duplication of chromosome 8(q13----q24.1) in a liveborn male.
    Donnenfeld AE, Coyne MD, Beauregard LJ.
    Am J Med Genet; 1990 Apr 01; 35(4):529-31. PubMed ID: 2333884
    [Abstract] [Full Text] [Related]

  • 10. A specific phenotype associated with trisomy 15 mosaicism.
    Fryns JP, Kleczkowska A, Lagae L, Kenis H, van den Berghe H.
    Ann Genet; 1993 Apr 01; 36(2):129-31. PubMed ID: 8215220
    [Abstract] [Full Text] [Related]

  • 11. A case of Alagille's syndrome with translocation (4;14) (q21;q21).
    Mujica P, Morali A, Vidailhet M, Pierson M, Gilgenkrantz S.
    Ann Genet; 1989 Apr 01; 32(2):117-9. PubMed ID: 2757361
    [Abstract] [Full Text] [Related]

  • 12. Trisomy for the distal part of the short arm of chromosome 3.
    Lurie IW, Korotkova IA, Zaletajev DV, Smirnova LI, Podlechshuk LV, Gurevich DB.
    Helv Paediatr Acta; 1986 Mar 01; 41(6):509-13. PubMed ID: 3583774
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
    Chen CP, Liu FF, Jan SW, Lin SP, Lan CC.
    Prenat Diagn; 1996 Mar 01; 16(3):270-5. PubMed ID: 8710784
    [Abstract] [Full Text] [Related]

  • 14. Monosomy 13q32.3----qter: report of two cases.
    Rivera H, González-Flores SA, Rivas F, Sánchez-Corona J, Moller M, Cantú JM.
    J Med Genet; 1985 Apr 01; 22(2):142-5. PubMed ID: 3989831
    [Abstract] [Full Text] [Related]

  • 15. Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features.
    Brueton LA, Barber JC, Huson SM, Winter RM.
    J Med Genet; 1989 Nov 01; 26(11):729-30. PubMed ID: 2479748
    [Abstract] [Full Text] [Related]

  • 16. The Wolf-Hirschhorn syndrome in fetuses.
    Tachdjian G, Fondacci C, Tapia S, Huten Y, Blot P, Nessmann C.
    Clin Genet; 1992 Dec 01; 42(6):281-7. PubMed ID: 1493641
    [Abstract] [Full Text] [Related]

  • 17. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun 01; 28(3):165-70. PubMed ID: 10964553
    [Abstract] [Full Text] [Related]

  • 18. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter).
    Chen CP, Lin SP, Chern SR, Lee CC, Chen LF, Chen YJ, Wang W.
    Genet Couns; 2006 Jun 01; 17(1):81-5. PubMed ID: 16719283
    [No Abstract] [Full Text] [Related]

  • 19. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH, van Bodegom TM, Moll HA, Govaerts LC.
    Ann Genet; 1999 Jun 01; 42(3):160-5. PubMed ID: 10526659
    [Abstract] [Full Text] [Related]

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