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Journal Abstract Search

323 related items for PubMed ID: 7395909

  • 1. The syndrome of ring chromosome 12.
    Scribanu N, McCullars EB, Baumiller RC, Colon AR.
    Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
    [Abstract] [Full Text] [Related]

  • 2. Brief clinical report: the dup(17p) syndrome.
    Feldman GM, Baumer JG, Sparkes RS.
    Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295
    [Abstract] [Full Text] [Related]

  • 3. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV, Kapstafer KJ, Lloyd MA.
    Am J Med Genet; 1980 Mar; 7(3):383-9. PubMed ID: 7468662
    [Abstract] [Full Text] [Related]

  • 4. Deletion of a portion of the long arm of chromosome 6.
    Goldberg R, Fish B, Ship A, Shprintzen RJ.
    Am J Med Genet; 1980 Mar; 5(1):73-80. PubMed ID: 7395903
    [Abstract] [Full Text] [Related]

  • 5. Chromosome 6/15 translocation with multiple congenital anomalies.
    Ming PM, Goodner DM, Park TS.
    Obstet Gynecol; 1977 Feb; 49(2):251-3. PubMed ID: 834413
    [Abstract] [Full Text] [Related]

  • 6. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU, Baumann WA.
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
    [Abstract] [Full Text] [Related]

  • 7. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [Abstract] [Full Text] [Related]

  • 8. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV, Driscoll DJ, Ledbetter DH, Riccardi VM.
    Am J Med Genet; 1981 Nov; 9(3):231-7. PubMed ID: 7025632
    [Abstract] [Full Text] [Related]

  • 9. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
    Kuleshov NP, Zaletaev DV, Levina LIa, Dement'eva GM, Arbuzov SP.
    Tsitol Genet; 1985 Nov; 19(6):452-6. PubMed ID: 4089954
    [Abstract] [Full Text] [Related]

  • 10. Balanced complex rearrangement involving chromosomes 8, 9, and 12 in a normal mother, derivative chromosome 9 with recombinant chromosome 12 in her daughter with minor anomalies.
    Masuno M, Asano J, Yasuda K, Kondo T, Orii T.
    Am J Med Genet; 1993 Jan 01; 45(1):65-7. PubMed ID: 8418663
    [Abstract] [Full Text] [Related]

  • 11. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM, Martin JA, Benjamin TR, Kukolich MK, Townsend-Parcham JK.
    Ann Genet; 1990 Jan 01; 33(3):173-5. PubMed ID: 2288463
    [Abstract] [Full Text] [Related]

  • 12. Ring chromosome 6: case report and review.
    Nishi Y, Yoshimura O, Ohama K, Usui T.
    Am J Med Genet; 1982 May 01; 12(1):109-14. PubMed ID: 7091194
    [Abstract] [Full Text] [Related]

  • 13. 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 May 01; 28(3):193-6. PubMed ID: 3879157
    [Abstract] [Full Text] [Related]

  • 14. Ring chromosome 17 in a mentally retarded boy.
    Qazi OH, Madahar C, Kanchanapoomi R, Giridharan R, Beller E.
    Ann Genet; 1979 May 01; 22(4):234-8. PubMed ID: 121681
    [Abstract] [Full Text] [Related]

  • 15. [A new case of trisomy 5p].
    Antonenko VG, Levina LIa, Chudnova VI.
    Genetika; 1985 Dec 01; 21(12):2066-70. PubMed ID: 4085794
    [Abstract] [Full Text] [Related]

  • 16. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P, Adkins WN, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C.
    Am J Med Genet; 1981 Dec 01; 10(2):159-77. PubMed ID: 7315873
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 18(1):5-11. PubMed ID: 1080038
    [Abstract] [Full Text] [Related]

  • 18. Ring chromosome 11 [46,XX,r(11) (p15q25)] associated with clinical features of the 11q- syndrome.
    Niikawa N, Jinno Y, Tomiyasu T, Fukushima Y, Kudo K.
    Ann Genet; 1981 Mar 01; 24(3):172-5. PubMed ID: 6974530
    [Abstract] [Full Text] [Related]

  • 19. Ring chromosome 22 and autism: report and review.
    MacLean JE, Teshima IE, Szatmari P, Nowaczyk MJ.
    Am J Med Genet; 2000 Feb 28; 90(5):382-5. PubMed ID: 10706359
    [Abstract] [Full Text] [Related]

  • 20. Girl with accelerated growth, hearing loss, inner ear anomalies, delayed myelination of the brain, and del(22)(q13.1q13.2).
    Fujita Y, Mochizuki D, Mori Y, Nakamoto N, Kobayashi M, Omi K, Kodama H, Yanagawa Y, Abe T, Tsuzuku T, Yamanouchi Y, Takano T.
    Am J Med Genet; 2000 May 29; 92(3):195-9. PubMed ID: 10817654
    [Abstract] [Full Text] [Related]

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