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Journal Abstract Search

378 related items for PubMed ID: 7205434

  • 1. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
    Stoll C, Levy J, Roth MP.
    J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
    [Abstract] [Full Text] [Related]

  • 2. Interstitial deletion of the short arm of chromosome 4.
    Ray M, Evans J, Rockman-Greenberg C, Wickstrom D.
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [Abstract] [Full Text] [Related]

  • 3. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990 Jun; 33(2):92-5. PubMed ID: 2241091
    [Abstract] [Full Text] [Related]

  • 4. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ, Planteydt HT, Hagemeijer A, Peters-Slough MF, Timmerman MJ.
    Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
    [Abstract] [Full Text] [Related]

  • 5. Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22).
    Ohdo S, Madokoro H, Hayakawa K.
    J Med Genet; 1982 Dec; 19(6):479. PubMed ID: 7154050
    [No Abstract] [Full Text] [Related]

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  • 7. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
    Caliebe A, Waltz S, Jenderny J.
    Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
    [Abstract] [Full Text] [Related]

  • 8. Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype.
    del Valle Torrado M, Labarta JD, Migliorini AM.
    J Med Genet; 1982 Dec; 19(6):477. PubMed ID: 6185682
    [No Abstract] [Full Text] [Related]

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  • 10. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M, Keppler-Noreuil K, Knops J, Longshore JW, Finley WH, Carroll AJ.
    Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
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  • 12. Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
    Glass IA, Swindlehurst CA, Aitken DA, McCrea W, Boyd E.
    J Med Genet; 1989 Feb; 26(2):127-30. PubMed ID: 2918541
    [Abstract] [Full Text] [Related]

  • 13. A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant.
    Park JP, Moeschler JB, Berg SZ, Bauer RM, Wurster-Hill DH.
    Clin Genet; 1992 Jan; 41(1):54-6. PubMed ID: 1633649
    [Abstract] [Full Text] [Related]

  • 14. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL, Cox BA, Kyine M, Uhlmann W, Glover TW.
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
    [Abstract] [Full Text] [Related]

  • 15. Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
    de Pablo CE, García Sagredo JM, Ferro MT, Ferrando P, San Román C.
    J Med Genet; 1980 Dec; 17(6):483-6. PubMed ID: 6937620
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B, Pilczer C, Dandine M, Tamboise A.
    Ann Genet; 1985 Nov; 28(4):251-3. PubMed ID: 3879441
    [Abstract] [Full Text] [Related]

  • 18. Chromosome 20 long arm deletion in an elderly malformed man.
    Shabtai F, Ben-Sasson E, Arieli S, Grinblat J.
    J Med Genet; 1993 Feb; 30(2):171-3. PubMed ID: 8445626
    [Abstract] [Full Text] [Related]

  • 19. Partial deletion of 4p16 band in a ring chromosome and Wolf Syndrome.
    del Mazo J, Abrisqueta JA, Pérez-Castillo A, Aller V, Lucas MA, de Torres ML, Martín MJ.
    Hum Genet; 1978 Oct 19; 44(1):105-8. PubMed ID: 711237
    [Abstract] [Full Text] [Related]

  • 20. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG, Bhola SL, Post-Blok CA, Hennekam RC, de France HF.
    Am J Med Genet; 1994 Nov 15; 53(3):296-9. PubMed ID: 7856666
    [Abstract] [Full Text] [Related]

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