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Journal Abstract Search

167 related items for PubMed ID: 464416

  • 1. ["Free" 9p trisomy in a male child with severe mental retardation (author's transl)].
    Aller V, Abrisqueta JA, Martín-Lucas MA, de Torres ML, del Mazo J, Pérez-Castillo A.
    An Esp Pediatr; 1979 May; 12(5):463-8. PubMed ID: 464416
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  • 2. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].
    Turleau C, De Grouchy J, Roubin M, Chavin-Colin F, Cachin O.
    Ann Genet; 1975 Jun; 18(2):125-9. PubMed ID: 1081365
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  • 3. [Partial trisomy 9 with partial retention of the long arm (author's transl)].
    Scheibenreiter S, Szilvássy J, Ender H.
    Wien Klin Wochenschr; 1976 Apr 16; 88(8):264-7. PubMed ID: 185815
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  • 4. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A.
    An Esp Pediatr; 1981 May 16; 14(5):344-51. PubMed ID: 7294523
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  • 5. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN, Yarbrough KM, Stoddard GR, Rary JM.
    Clin Genet; 1977 Jan 16; 11(1):46-52. PubMed ID: 830449
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  • 6. [Partial trisomy 11q;22q (author's transl)].
    Benítez J, Ayuso C, García Aparicio J, Sáez E, Pérez Sotelo A, Bello MJ.
    An Esp Pediatr; 1981 Sep 16; 15(3):293-300. PubMed ID: 7332142
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  • 10. [Partial 7 q trisomy. One or 2 syndromes? Apropos of a new case].
    Turleau C, Rossier A, de Montis G, Roubin M, Chavin-Colin F, de Grouchy J.
    Ann Genet; 1976 Mar 16; 19(1):37-42. PubMed ID: 1084120
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  • 11. C8 trisomy mosaicism syndrome.
    Bijlsma JB, Wijffels JC, Tegelaers WH.
    Helv Paediatr Acta; 1972 Jul 16; 27(3):281-98. PubMed ID: 4645654
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  • 12. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG, Gracia R, López Pajares I, González M, Oliver A, Peralta A.
    An Esp Pediatr; 1982 Aug 16; 17(2):125-9. PubMed ID: 7149479
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  • 13. [Ring 6-chromosome: a nonspecific clinical picture].
    Sele B, Joannard A, Jalbert P, Boucharlat J.
    Ann Genet; 1977 Dec 16; 20(4):232-6. PubMed ID: 305748
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  • 16. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
    Coco R, Penchaszadeh VB.
    J Genet Hum; 1978 Sep 16; 26(3):203-10. PubMed ID: 739260
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  • 19. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun 16; 17(2):119-24. PubMed ID: 4547939
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