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Journal Abstract Search

275 related items for PubMed ID: 5205520

  • 1. [A single D chromosome in ring form in a 2-year-old girl with mental retardation].
    Morić-Petrović S, Garzicić B, Despotović M, Kalicanin P.
    Srp Arh Celok Lek; 1970 Mar; 98(3):447-52. PubMed ID: 5205520
    [No Abstract] [Full Text] [Related]

  • 2. [49, XXXXX syndrome in a 5-year-old girl].
    Larget-Piet L, Rivron J, Baillif P, Dugay J, Emerit I, Larget-Piet A, Berthelot J.
    Ann Genet; 1972 Jun; 15(2):115-9. PubMed ID: 4537723
    [No Abstract] [Full Text] [Related]

  • 3. Aberrant serum protein inheritance in a patient with a ring D chromosome.
    Daniel WL.
    Pediatrics; 1970 Jul; 46(1):120-3. PubMed ID: 5423439
    [No Abstract] [Full Text] [Related]

  • 4. Autosomal dominant microcephaly with mental retardation.
    Bawle E, Horton M.
    Am J Med Genet; 1989 Jul; 33(3):382-4. PubMed ID: 2801773
    [Abstract] [Full Text] [Related]

  • 5. [Ring chromosome D13-case history and survey (author's transl)].
    Zink U, Rix R, Grosse KP, Schwanitz G.
    Klin Padiatr; 1973 May; 185(3):192-7. PubMed ID: 4795573
    [No Abstract] [Full Text] [Related]

  • 6. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.
    Jenkins EC, Curcuru-Giordano FM, Krishna SG, Cantarella J.
    Ann Genet; 1975 Jun; 18(2):117-20. PubMed ID: 1081364
    [Abstract] [Full Text] [Related]

  • 7. [Ring formation of Chromosome 18. Case report and review of the literature].
    Cortesi M, Patriarca PL.
    Minerva Pediatr; 1971 May 19; 23(30):902-8. PubMed ID: 5570156
    [No Abstract] [Full Text] [Related]

  • 8. Ring chromosome 15 syndrome.
    Fryns JP, Jaeken J, Devlieger H, Debucquoy P, Eggermont E, Van den Berghe H.
    Acta Paediatr Belg; 1981 May 19; 34(1):47-9. PubMed ID: 7270144
    [No Abstract] [Full Text] [Related]

  • 9. Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34).
    Hernandez A, Garcia-Cruz D, Plascencia L, Nazara Z, Rivera H, Sanchez-Corona J, Cantu JM.
    Ann Genet; 1979 May 19; 22(4):221-4. PubMed ID: 317785
    [Abstract] [Full Text] [Related]

  • 10. [A patient with ring chromosome 13].
    Hammond A, Bijlsma JB.
    Ned Tijdschr Geneeskd; 1981 May 09; 125(19):752-5. PubMed ID: 7242723
    [No Abstract] [Full Text] [Related]

  • 11. [Crying cat syndrome discovered during a routine examination].
    Lafon R, Emberger JM, Pouget R, Chiariny JF.
    Ann Med Psychol (Paris); 1972 May 09; 2(3):431-8. PubMed ID: 4675135
    [No Abstract] [Full Text] [Related]

  • 12. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 09; 15(5):469-73. PubMed ID: 7332149
    [Abstract] [Full Text] [Related]

  • 13. Association of hypertelorism and hypospadias--the BBB-syndrome.
    Michaelis E, Mortier W.
    Helv Paediatr Acta; 1972 Dec 09; 27(6):575-81. PubMed ID: 4405408
    [No Abstract] [Full Text] [Related]

  • 14. [Deficiency of the long arm of chromosome no. 18 (46,XX,18q-)].
    Cenani A, Schoeller L, Schubart G.
    Arch Kinderheilkd; 1969 Mar 09; 178(3):266-72. PubMed ID: 5800650
    [No Abstract] [Full Text] [Related]

  • 15. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Schwanitz G, Schamberger U, Rott HD, Wieczorek V.
    Ann Genet; 1974 Sep 09; 17(3):163-6. PubMed ID: 4548816
    [No Abstract] [Full Text] [Related]

  • 16. [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 09; 15(4):383-9. PubMed ID: 7337304
    [No Abstract] [Full Text] [Related]

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