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Journal Abstract Search

355 related items for PubMed ID: 4139262

  • 1. Inherited partial duplication of chromosome No. 15.
    Fujimoto A, Towner JW, Ebbin AJ, Kahlstrom EJ, Wilson MG.
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
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  • 3. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Sep; 23(6):568-85. PubMed ID: 4134631
    [No Abstract] [Full Text] [Related]

  • 4. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS, McKusick VA, Farber PA.
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
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  • 6. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E, Pfeiffer RA.
    Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177
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  • 7. A retarded child with a 46XX,3p-q+ chromosome karyotype.
    Butler LJ, Hall ME, Wharton BA.
    J Ment Defic Res; 1974 Mar; 18(0):41-9. PubMed ID: 4424443
    [No Abstract] [Full Text] [Related]

  • 8. Familial mental retardation in a family with an inherited chromosome rearrangement.
    Chudley AE, Bauder F, Ray M, McAlpine PJ, Pena SD, Hamerton JL.
    J Med Genet; 1974 Dec; 11(4):353-66. PubMed ID: 4140909
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  • 9. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A, Tenconi R, Baccichetti C, Pujatti G.
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract] [Full Text] [Related]

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  • 11. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Jul; 24(1):100-4. PubMed ID: 4136482
    [No Abstract] [Full Text] [Related]

  • 12. Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies.
    Carrel RE, Sparkes RS, Wright SW.
    J Pediatr; 1971 Apr; 78(4):664-72. PubMed ID: 5547823
    [No Abstract] [Full Text] [Related]

  • 13. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974 Apr; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 14. Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.
    Waldenmaier C, Hirsch W, König E, Shibata K.
    Humangenetik; 1974 Mar 28; 21(4):323-9. PubMed ID: 4134628
    [No Abstract] [Full Text] [Related]

  • 15. A child with a ring-4 chromosome (46,XX-46,XX,r 4).
    Parker CE, Alfi OS, Derencsenyi A, Mavalwala J, Donnell G.
    Am J Dis Child; 1974 Sep 28; 128(3):371-4. PubMed ID: 4411581
    [No Abstract] [Full Text] [Related]

  • 16. A possible case of partial trisomy for chromosome 22: further evidence from Giemsa banding studies.
    Sands ME.
    J Ment Defic Res; 1974 Dec 28; 18(4):327-30. PubMed ID: 4142949
    [No Abstract] [Full Text] [Related]

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  • 18. 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 28; 130(6):663-7. PubMed ID: 937286
    [Abstract] [Full Text] [Related]

  • 19. Partial monosomy 13 and 21 due to a familial 13/21 translocation.
    Otto PG, Toledo S, Richieri-Costa A, Otto PA, Vianna-Morgante AM, Kasahara S.
    Hum Genet; 1978 Apr 24; 41(3):243-50. PubMed ID: 649151
    [Abstract] [Full Text] [Related]

  • 20. Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.
    Funderburk SJ, Crandall BF.
    Am J Hum Genet; 1974 Nov 24; 26(6):715-22. PubMed ID: 4140688
    [No Abstract] [Full Text] [Related]

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