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Journal Abstract Search

163 related items for PubMed ID: 3621644

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation.
    Behjati F, Shafeghati Y, Kahrizi K, Firouzabadi SG, Najmabadi H, Dixon N, Davies AF.
    Am J Med Genet A; 2008 Dec 15; 146A(24):3223-6. PubMed ID: 19012333
    [No Abstract] [Full Text] [Related]

  • 3. Deletion of chromosome 2 (p11-p13): case report and review.
    Prasher VP, Krishnan VH, Clarke DJ, Maliszewska CT, Corbett JA.
    J Med Genet; 1993 Jul 15; 30(7):604-6. PubMed ID: 8411037
    [Abstract] [Full Text] [Related]

  • 4. Chromosome 20 long arm deletion in an elderly malformed man.
    Shabtai F, Ben-Sasson E, Arieli S, Grinblat J.
    J Med Genet; 1993 Feb 15; 30(2):171-3. PubMed ID: 8445626
    [Abstract] [Full Text] [Related]

  • 5. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
    Silengo MC, Davi GF, Bianco R, Biagioli M, Guala A, Franceschini P, Novelli G.
    Clin Genet; 1984 Jun 15; 25(6):549-52. PubMed ID: 6587954
    [Abstract] [Full Text] [Related]

  • 6. A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p.
    Uehara S, Akai Y, Takeyama Y, Okamura K, Takabayashi T, Yajima A, Natsui M, Nakai H.
    Clin Genet; 1993 Jan 15; 43(1):28-33. PubMed ID: 8179640
    [Abstract] [Full Text] [Related]

  • 7. The 18 p- syndrome: report of one case.
    Wang SF, Lin SP, Shen EY, Yang SY.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994 Jan 15; 35(1):78-83. PubMed ID: 8178647
    [Abstract] [Full Text] [Related]

  • 8. Aniridia caused by a heritable chromosome 11 deletion.
    Hittner HM, Riccardi VM, Francke U.
    Ophthalmology; 1979 Jun 15; 86(6):1173-83. PubMed ID: 230439
    [Abstract] [Full Text] [Related]

  • 9. Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype.
    Khalifa MM, MacLeod PM, Duncan AM.
    Clin Genet; 1993 Nov 15; 44(5):258-61. PubMed ID: 7906212
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 41(1):54-6. PubMed ID: 1633649
    [Abstract] [Full Text] [Related]

  • 11. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies.
    Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.
    Hum Genet; 1983 Jan 15; 64(1):97. PubMed ID: 6873944
    [No Abstract] [Full Text] [Related]

  • 12.
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    [No Abstract] [Full Text] [Related]

  • 13. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
    Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.
    Hum Genet; 1983 Jan 15; 64(1):98. PubMed ID: 6873945
    [No Abstract] [Full Text] [Related]

  • 14. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A, Cain R, Howell R.
    Hum Genet; 1980 Jan 15; 53(3):305-7. PubMed ID: 7372333
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 50(6):538-40. PubMed ID: 9147894
    [Abstract] [Full Text] [Related]

  • 16. Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
    Trautmann U, Pfeiffer RA, Seufert-Satomi U, Tietze HU.
    J Med Genet; 1993 Apr 15; 30(4):330-1. PubMed ID: 8487285
    [Abstract] [Full Text] [Related]

  • 17.
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    [No Abstract] [Full Text] [Related]

  • 18. 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 15; 17(6):486-7. PubMed ID: 7205434
    [Abstract] [Full Text] [Related]

  • 19. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP, Kleczkowska A, van den Berghe H.
    Clin Genet; 1988 Jan 15; 33(1):60-2. PubMed ID: 3342549
    [Abstract] [Full Text] [Related]

  • 20. A case of de novo interstitial deletion 3q.
    Okada N, Hasegawa T, Osawa M, Fukuyama Y.
    J Med Genet; 1987 May 15; 24(5):305-8. PubMed ID: 3585947
    [Abstract] [Full Text] [Related]

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