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Journal Abstract Search

208 related items for PubMed ID: 6681937

  • 1. Duplication (17p) in a child with an isodicentric (17p) chromosome.
    Mascarello JT, Jones MC, Hoyme HE, Freebury MM.
    Am J Med Genet; 1983 Jan; 14(1):67-72. PubMed ID: 6681937
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  • 2. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
    Elejalde BR, Opitz JM, de Elejalde MM, Gilbert EF, Abellera M, Meisner L, Lebel RR, Hartigan JM.
    Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
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  • 3. De novo partial 2p duplication with postmortem description.
    Monteleone PL, Blair JD, Graviss ER, Chen SC, Salvador A, Grzegocki JA, Monteleone JA.
    Am J Med Genet; 1981 Apr; 10(1):55-64. PubMed ID: 7197468
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  • 4. Monosomy 21: a possible stepwise evolution of the karyotype.
    Abeliovich D, Carmi R, Karplus M, Bar-Ziv J, Cohen MM.
    Am J Med Genet; 1979 Apr; 4(3):279-86. PubMed ID: 574719
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  • 5. Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter).
    Passarge E, Bartsch-Sandhoff M, Rehder H.
    Teratology; 1982 Apr; 25(2):221-5. PubMed ID: 7101200
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  • 6. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
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  • 12. Brief clinical report: deletion of the long arm of chromosome 11, [del(11)(q23)].
    Monteleone PL, Chen SC, Nouri-Moghaddam S, Blair JD, Tietjens M.
    Am J Med Genet; 1982 Nov 15; 13(3):299-304. PubMed ID: 6891182
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  • 14. De novo duplication of 17p [dup(17)(p12----p11.2)]: report of an additional case with confirmation of the cytogenetic, phenotypic, and developmental aspects.
    Kozma C, Meck JM, Loomis KJ, Galindo HC.
    Am J Med Genet; 1991 Dec 15; 41(4):446-50. PubMed ID: 1776635
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