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Journal Abstract Search

226 related items for PubMed ID: 4136482

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

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

  • 3. An 18p21q translocation in a patient with presumptive "monosomy G".
    Cohen MM, Putnam TI.
    Am J Dis Child; 1972 Dec; 124(6):908-10. PubMed ID: 4639227
    [No Abstract] [Full Text] [Related]

  • 4. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O, Yunis JJ, Escobar JI.
    Humangenetik; 1974 Apr 24; 22(1):59-65. PubMed ID: 4134840
    [No Abstract] [Full Text] [Related]

  • 5. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ.
    Neurology; 1973 Nov 24; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract] [Full Text] [Related]

  • 6. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Rethoré MO, Hoehn H, Rott HD, Couturier J, Dutrillaux B, Lejeune J.
    Humangenetik; 1973 Apr 16; 18(2):129-38. PubMed ID: 4124236
    [No Abstract] [Full Text] [Related]

  • 7. [A single D chromosome in ring form in a 2-year-old girl with mental retardation].
    Morić-Petrović S, Garzicić B, Despotović M, Kalicanin P.
    Srp Arh Celok Lek; 1970 Mar 16; 98(3):447-52. PubMed ID: 5205520
    [No Abstract] [Full Text] [Related]

  • 8. Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl.
    Fryns JP, Verresen H, Van den Berghe H.
    Humangenetik; 1974 Mar 16; 24(3):241-6. PubMed ID: 4140835
    [No Abstract] [Full Text] [Related]

  • 9.
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    [No Abstract] [Full Text] [Related]

  • 10. 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 Mar 16; 23(6):568-85. PubMed ID: 4134631
    [No Abstract] [Full Text] [Related]

  • 11. [Monosomy of chromosome 21].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1983 Jun 16; 58(6):557-9. PubMed ID: 6646915
    [No Abstract] [Full Text] [Related]

  • 12. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E, Pfeiffer RA.
    Hum Genet; 1979 Nov 16; 52(2):217-20. PubMed ID: 511177
    [Abstract] [Full Text] [Related]

  • 13. Inherited partial duplication of chromosome No. 15.
    Fujimoto A, Towner JW, Ebbin AJ, Kahlstrom EJ, Wilson MG.
    J Med Genet; 1974 Sep 16; 11(3):287-91. PubMed ID: 4139262
    [Abstract] [Full Text] [Related]

  • 14. Ring chromosome 13 syndrome.
    Fried K, Rosenblatt M, Mundel G, Krikler R.
    Clin Genet; 1975 Mar 16; 7(3):203-8. PubMed ID: 1139790
    [Abstract] [Full Text] [Related]

  • 15. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M, Schmid E, Röttinger E.
    Humangenetik; 1968 Mar 16; 6(4):303-10. PubMed ID: 5713616
    [No Abstract] [Full Text] [Related]

  • 16. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE, Appadorai V, Breg WR, Howard RO.
    Birth Defects Orig Artic Ser; 1974 Mar 16; 10(8):19-25. PubMed ID: 4142400
    [No Abstract] [Full Text] [Related]

  • 17. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF, Weber F, Muller HM, Burwell JK.
    Clin Genet; 1972 Mar 16; 3(4):264-70. PubMed ID: 5054320
    [No Abstract] [Full Text] [Related]

  • 18. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
    Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF.
    Eur J Pediatr; 2008 Jun 16; 167(6):655-9. PubMed ID: 17668239
    [Abstract] [Full Text] [Related]

  • 19. Indications for chromosome analysis illustrated by a case of ring 22.
    Howard-Peebles PN.
    J Hered; 1977 Jun 16; 68(4):268-9. PubMed ID: 411817
    [Abstract] [Full Text] [Related]

  • 20. X-chromosome banding in Noonan syndrome.
    Barlow MJ, Neu RL, Gardner LI.
    Am J Dis Child; 1973 Nov 16; 126(5):656-7. PubMed ID: 4126797
    [No Abstract] [Full Text] [Related]

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