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Journal Abstract Search

254 related items for PubMed ID: 6646915

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

  • 2. [Identification of an unusual chromosome anomaly in a malformative syndrome].
    Vianello MG, De Prà M.
    Minerva Pediatr; 1969 Apr 14; 21(15):611-8. PubMed ID: 5402255
    [No Abstract] [Full Text] [Related]

  • 3. 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 Apr 14; 10(8):19-25. PubMed ID: 4142400
    [No Abstract] [Full Text] [Related]

  • 4. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS, Murthy SK, Banker GJ, Patel AJ.
    Indian Pediatr; 1991 May 14; 28(5):546-9. PubMed ID: 1684352
    [No Abstract] [Full Text] [Related]

  • 5. [Familial Russell-syndrome (author's transl)].
    Schwingshackl A, Ganner E, Hammerer I.
    Padiatr Padol; 1974 May 14; 9(2):130-7. PubMed ID: 4823694
    [No Abstract] [Full Text] [Related]

  • 6. [Trisomy 4p. A case presentation (author's transl)].
    Delgado A, Egüés J, Muñoz M, González Villa P, Bernaola E, del Amo A.
    An Esp Pediatr; 1981 Oct 14; 15(4):383-9. PubMed ID: 7337304
    [No Abstract] [Full Text] [Related]

  • 7. [Partial trisomy of chromosome 22 in an infant].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1983 Jun 14; 58(6):561-4. PubMed ID: 6646916
    [No Abstract] [Full Text] [Related]

  • 8. 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 Jun 14; 4(3):279-86. PubMed ID: 574719
    [Abstract] [Full Text] [Related]

  • 9. [Tendency for chromosome breaks in Russel's syndrome].
    Ganner E, Schwingshackl A.
    Klin Wochenschr; 1970 May 15; 48(10):629-32. PubMed ID: 5517331
    [No Abstract] [Full Text] [Related]

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  • 16. [Chromosome 8 trisomy in an infant].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1982 May 15; 57(5-6):425-7. PubMed ID: 7155694
    [No Abstract] [Full Text] [Related]

  • 17. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
    Badalian LO, Malygina NA, Gozman TV, Petrukhin AS, Mutovin GR.
    Tsitol Genet; 1982 May 15; 16(2):17-21. PubMed ID: 7101445
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