These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 6646916

  • 41. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV, Carpenter NJ, Gucsavas M, Coldwell J, Say B.
    Am J Med Genet; 1995 Jul 31; 58(1):50-3. PubMed ID: 7573156
    [Abstract] [Full Text] [Related]

  • 42. Acrofacial dysostosis with ambiguous genitalia.
    Wulfsberg EA, Curtis J, Wiswell TE, Puntel RA, Levin SW.
    Am J Med Genet; 1990 Nov 31; 37(3):384-7. PubMed ID: 2260569
    [Abstract] [Full Text] [Related]

  • 43. The Aarskog syndrome in three brothers.
    Funderburk SJ, Crandall BF.
    Clin Genet; 1974 Nov 31; 6(2):119-24. PubMed ID: 4430151
    [No Abstract] [Full Text] [Related]

  • 44. [C trisomy].
    Berger R.
    Nouv Presse Med; 1972 Apr 01; 1(14):951-2. PubMed ID: 5026113
    [No Abstract] [Full Text] [Related]

  • 45. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG, Zackowski JL, Storto PD, Newlin A.
    Am J Med Genet; 1996 Jun 14; 63(3):434-7. PubMed ID: 8737648
    [Abstract] [Full Text] [Related]

  • 46. The leopard (multiple lentigines) syndrome revisited.
    Gorlin RJ, Anderson RC, Moller JH.
    Laryngoscope; 1971 Oct 14; 81(10):1674-81. PubMed ID: 4398858
    [No Abstract] [Full Text] [Related]

  • 47. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Oct 14; 24(1):100-4. PubMed ID: 4136482
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J, Cabrerizo Portero D, Montserrat Bernal F, Rodríguez Costa T, Cabrerizo Merino C, Rodríguez López F.
    An Esp Pediatr; 1981 Dec 14; 15(6):587-91. PubMed ID: 7337311
    [Abstract] [Full Text] [Related]

  • 53.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55. Two sibs with partial trisomy 2q.
    Barnicoat AJ, Abusaad I, Mackie CM, Robards MF.
    Am J Med Genet; 1997 May 16; 70(2):166-70. PubMed ID: 9128937
    [Abstract] [Full Text] [Related]

  • 56. [Aarskog's genito-digito-facial syndrome].
    Fouanon C, André MJ, Gillot F.
    Bull Soc Ophtalmol Fr; 1976 Nov 16; 76(11):981-5. PubMed ID: 1030364
    [No Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. Partial proximal trisomy 10q syndrome: a new case.
    Nucaro A, Faedda A, Cao A, Boccone L.
    Genet Couns; 2002 Nov 16; 13(4):411-6. PubMed ID: 12558111
    [Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 8.